Category Manager

Top Horizontal Menu Skip to main content Alt + 1 Skip to page footer Alt + 2 Menu , Home Page Options Jobs Location Search Assistance Sign In Hide sub menu Hide Dashboard Alerts Accessibility Home My Dashboard Job Details Top Job Details Here are the details for the selected job. You may need to scroll down to see all the information about the job, including the job description. If you wish to apply for this job click on the Apply button.

WARNING:

Always be on the lookout for job scams! Learn more about identity theft Opens in new window First Job Previous Job 781 of 6,435 Next Job Last Job Share More Like This Between $109k and $149k Per Year DOE (Depends on Experience) Category Manager Bachem Americas, Inc.

Occupation:

Purchasing Managers

Location:

VISTA, CA - 92081

Positions available: 1 Job #: 19846139

Source:

CalJOBS

Posted:

03/30/2026

Updated:

04/01/2026

Expires:

05/05/2026

Web Site:

CalJOBS Onsite /

Remote:

Not Specified

Job Type:

Regular, Full Time (30 Hours or More), Permanent Employment Job Requirements and Properties Help for Job Requirements and Properties. Opens a new window. Work Onsite Full Time Education Bachelor's Degree Experience 3 Month(s) Schedule Full Time Job Type Regular Duration Permanent Employment Public Transit Available Benefits Job Description Help for Job Description. Opens a new window. A brief overview The Category Manager oversees direct materials procurement, with a primary focus on chemicals, primary packaging, and external laboratory services. This role is accountable for developing and executing category and sourcing strategies, issuing purchase orders, and maintaining robust risk-mitigation plans. The ideal candidate will have established strong supplier relationships within these categories and possess solid contracting experience. What you will do Define a supplier relationship management program, including segmentation criteria and a preferred supplier list for a given category Develop and execute a 3-5 year strategic plan to realize category strategy targets Conduct market and competitive conditions by category Develop cost saving targets for each category Deliver customer solutions via global/regional category strategy Bring Industry/business function-specific knowledge and experience Responsible for developing and executing Sourcing Strategies, leading Sourcing Events-e.g. RFP, and the negotiation and contracting of supply agreements with strategic terms and conditions Initiate/build industry peer relationships Drive co-ownership of initiatives and accountability based on agreed-upon strategies Foster collaborative relationships with highly strategic global/regional suppliers Identify, build, and maintain mutually beneficial relationships, partnerships, and alliances with strategic and bottleneck suppliers through Supplier Relationship programs Responsible for assessing supplier risks and materials and recommending risk mitigation plans Develop a list of strategic and bottleneck suppliers within a category of spend and manage compliance Recommend or implement changes to the organization's purchasing, supply management and material usage policies as needed Measure supplier performance using rating systems or predetermined standards Process purchase orders based on SAP-MRP reports for raw materials and technical components, or purchase requisitions for non-inventory acquisitions Work with the suppliers and logistics to ensure on-time delivery to meet all scheduling requirements Maintains accurate and up-to-date information on purchase orders including price, terms, quantity and delivery date. Process SAP-MRP exception messages as required Communicates in a timely fashion, all information regarding raw material sourcing, pricing, delivery date changes, results, etc. to appropriate individuals in Material Management, Planning, R D, and others as necessary Resolve non-conformance items through internal and external processes. Ensure rejected material is returned to suppliers within established guidelines and that credits/replacement are received on time when appropriate Working closely with Material Management and Accounts-Payable teams to make sure all Good Receipts and Invoices are posted against Purchase Orders Lead cross-functional teams to drive results on category, sourcing, supplier risk activities Contribute continuous improvements to achieve higher levels of business value Qualifications Bachelor's degree in life sciences, business, or related field. Master's degree or MBA (preferred) 3+ experience in strategic procurement in any industry or Any other related bachelor's degree with 5+ years of experience in strategic procurement in the Pharmaceutical/Biotech industry Experience with Peptides (preferred) SAP system experience (preferred) Demonstrated experience in identifying and utilizing full set of sourcing levers to drive value for customers Exceptional understanding and application of Procurement principles, concepts, practices, and standards (i.e. effective negotiation, supplier relationship management, business partnering, supplier diversity etc.) along with an in-depth knowledge of industry practices Ability to conduct benchmarking to address cost, quality, risk and innovation considerations Ability to establish credibility and influence with diverse audiences and be perceived as a lead/influencer Able to develop solutions to complex problems that require an in-depth degree of ingenuity, creativity and innovativeness Independent self-starter and able to motivate others to accomplish ambiguous tasks Ability to lead teams in a matrix organization, across geographic and functional reporting lines Demonstrated track record of identifying root causes to issues and proactively problem solving Change management experience with large and complex organizational transformations Demonstrated success in partnering cross-functionally Ability to own and strengthen relationships with key customers and to champion change Compelling and persuasive communicator (oral and written) with excellent interpersonal and presentation skills to work across functions, sites, and geographies Knowledge of cGMP and FDA regulations Certified in Logistics, Transportation, and Distribution (CLTD)-APICS (preferred) CPSM or related certification (preferred) Bachem Americas, Inc. Is a Private Sector employer with 5 locations http://www.bachem.com

Company Profile:

(Confidential) Did Not Disclose Number of Employees Connect with Bachem Americas, Inc. Other Local Jobs from Bachem Americas, Inc. Help for Other Local Jobs from. Opens a new window. Change to Grid view Pause Carousel Previous Slide Next Slide Slide 1 Slide 2 Slide 3 Production Coach Bachem Americas, Inc. Vista, CA Coaches and Scouts Regular | $83,680.00-$115,060.00 Year Corporate - 1 week ago Production Coach Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. A brief overview The Production Coach provides daily leadership, technical guidance, and operational support to an assigned manufacturing team. This role oversees all activities within the work area to ensure production schedules, performance targets, and project deadlines are met in full compliance with cGMP standards. Responsibilities include training team members on equipment operation, applying chemistry expertise to troubleshoot issues, and reviewing documentation for accuracy and adherence to policies and procedures, including timekeeping, EHS requirements, and 5S practices. The Production Coach ensures effective communication across shifts, maintains consistent operational handoffs, and drives continuous improvement initiatives to reduce waste and enhance efficiency. What you will do

• Execute and support assigned production stages such as synthesis, cleavage, cyclization, conjugation, purification, reconstitution, lyophilization and in-process analytics. Sign off on steps requiring supervision, diagnose and troubleshoot equipment issues, make data-based decisions and escalate to appropriate parties when necessary.
• Provide technical training and guidance on equipment, BPR, SOPs, STMs, utilization, Safety standards, 5S standards, compliance, etc. and chemistry processes to support the ongoing development of each member of the team. Ensures that all team member Master Control requirements are met in a timely manner. Maintains training and certification records for team members, as needed.
• Install, operate and maintain equipment for production and in-process testing. The equipment includes but is not limited to analytical HPLC/UPLC, prep. HPLC systems, lyophilizes, balances, reactors, HF cleavage equipment, diafiltration systems, water purification systems, ovens, washing systems and others used in manufacturing.
• Schedule work assignments and ensure team members are able to take timely rest breaks and meal periods and that all applicable hours are accurately captured on work orders. Stand in for team members to cover breaks or lunches to ensure that a process continues, as needed.
• Ensure operations are running efficiently, and safety & compliance requirements are met through active monitoring of operations in the suites.
• Provide and ensure safe & efficient use of instruments, raw materials and other resources while scheduling production activities and communicating with all responsible departments involved.
• Review BPRs, logbooks, other quality documents, as needed, but at least once daily. Act as a witness to procedures as required. Provide constructive feedback and coaching to their team members regarding performance.
• Initiate, investigate and close quality events (Deviation, CAPA, etc.) in a timely manner. Support investigations and implementation of corrective actions with technical knowledge.
• Ensure seamless transfer of information and responsibilities across shifts and between areas. Plan, attend and lead production huddles meetings representing production team, bringing knowledge of processes, equipment and schedule, as needed.
• Regularly identify improvement initiatives and involve team members in ongoing improvement activities.

General Requirements (Outer) Skills (Inner) Specialized (Center) 0% Occupation 0% Education 0% Work Experience 0% Location 0% Salary N/A Job Skills N/A Shift N/A Min. Age N/A Drivers Lic. N/A DL Endorsements N/A Typing N/A Security Clearance N/A Language This chart is used to compare your background against this job to help to determine if you would be a good fit for this position. You match 0% of the General Job Requirements. You match 0% of the Skills Required, and you match 0% of the Specialized Job Requirements. End of interactive chart. View Share Technical Writer Bachem Americas, Inc. Vista, CA Technical Writers Regular Corporate - 1 week ago All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status Bachem Americas, Inc. Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. A brief overview The Technical Writer I will prepare cGMP documentation, including protocols, reports, studies, Failure Mode and Effect Analyses (FMEAs), memos, forms, specifications, qualifications, change controls, deviations, Corrective and Preventative Actions (CAPA), Standard Operating Procedures (SOPs), and Master Batch Production Records (MBPRs). What you will do

• Write and revise documentation, such as protocols, reports, SOPs and associated forms, and MBPRs. Review and complete all documentation following cGMP guidelines
• Ensure collaboration between all applicable departments, such as Production, Facilities, Materials Management, QA and QC
• Adhere to manufacturing schedules and timelines
• Participate in the validation of products and processes
• Participate in project meetings with subject material experts Qualifications
• Bachelor's Degree BS Degree in Chemistry or related field
• Minimum of 1 year of work experience as a chemist or scientist in a cGMP environment
• 1 year of technical writing experience
• Experience with peptide manufacturing and associated analytical methods
• Experience with cGMP manufacturing and documentation standards (Preferred)
• Understanding of in-process analytical methods (e.g. HPLC)
• Comfortable working around hazardous materials and chemicals
• Excellent written and oral communication skills
• Basic computer knowledge, including Microsoft Word, Excel and PowerPoint
• Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment
• Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues
• Detail oriented with the ability to troubleshoot and resolve problems
• Ability to work independently and manage one's time
• Ability to communicate effectively and function well in a team environment

Base Salary Range:

Technical Writer I:

$61,171.20-$84,110.40

Technical Writer II:

$67,655.26-$93,025.98

Technical Writer III:

$82,136.80-112,938.10 Placement of new hires in this wage range is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees' environmental awareness.

EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. ???????????Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. Equal employment opportunity, including veterans and individuals with disabilities.

PI283442892

General Requirements (Outer) Skills (Inner) Specialized (Center) 0% Occupation 0% Education 0% Work Experience 0% Location 0% Salary N/A Job Skills N/A Shift N/A Min. Age N/A Drivers Lic. N/A DL Endorsements N/A Typing N/A Security Clearance N/A Language This chart is used to compare your background against this job to help to determine if you would be a good fit for this position. You match 0% of the General Job Requirements. You match 0% of the Skills Required, and you match 0% of the Specialized Job Requirements. End of interactive chart. View Share Manager / Sr. Manager, Quality Control Bachem Americas, Inc. Vista, CA Management Occupations Regular Corporate - 1 week ago All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status Bachem Americas, Inc. Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. A brief overview The Manager / Sr. Manager, Quality Control fulfills a critical role in the active pharmaceutical ingredient (API) manufacturing operations. This individual is responsible for managing and coordinating stability testing, raw material qualification, testing and release, and validation projects. The Manager / Sr. Manager coordinates both in-house and contract laboratory testing activities. Additionally, this individual supports the Director, Quality Control in reviewing data and reports. This role also serves to advance analytical capabilities and contributes to the development of the Quality Control department. What you will do

• Manage and oversee execution of QC testing including IPC, API, raw material, validation, release, EM and microbial testing
• Supervise QC Scientists. Provide training, day-to-day scheduling, mentoring, and coaching for QC personnel
• Establish and revise specifications and sampling plans for IPC, raw materials and final product
• Develop and optimize new and existing analytical methods for qualification and release testing
• Coordinate stability program and the testing to meet stability endpoints, as needed
• Manage IPC release activities, raw material and API release activities to meet deadlines tied to manufacturing schedules
• Write, review, and approve QC Standard Operating procedures (SOP's) as needed
• Evaluate, recommend, and implement new analytical technologies and instrumentation for raw material, final product, In process, microbial, environmental, and water testing
• Investigate Out-Of-Specification (OOS) test results, write reports and implement corrective and preventive actions (CAPA) to prevent recurrences
• Manage external test laboratories for contract testing of raw materials and other related testing
• Review test data for completeness and accuracy
• Provide timely responses to internal and external inquiries
• Stay abreast of new developments in analytical technologies
• Contribute to improvements in laboratory operations to increase efficiency and GMP compliance Qualifications
• Bachelor's degree in a relevant scientific field with a minimum of 8 years' industry experience
• Master's degree in a relevant scientific field with a minimum of 5 years' industry experience (preferred)
• PhD in a relevant scientific field with a minimum of 2 years' industry experience (preferred)
• 1-3 years' management experience (preferred)
• 1-3 years' experience in managing projects (preferred)
• Extensive experience in GMP laboratory testing such as

IPC, HPLC, GC, TLC, UV-VIS

Spectrophotometer, Karl Fisher Titrator, FTIR, MS, LAL, bioburden, etc.

• Thorough knowledge and understanding of analytical chemistry, including USP materials testing
• Creativity to solve technical and compliance problems
• Comply with good housekeeping and safety practices
• Experience in writing standard operating procedures (SOP's) and test methods
• Excellent written and oral communication skills
• Excellent computer knowledge, including Microsoft Word, Excel, Power Point and Access
• Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment
• Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues
• Detail oriented with the ability to troubleshoot and resolve problems
• Ability to work independently and manage one's time
• Ability to drive projects to success under time constraints
• Communicate effectively and ability to function well in a team environment Base salary range:

Manager:

$109,396 - $164,095 Sr.

Manager:

$133,304 - $183,293?Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. ?Corporate Social Responsibility ?Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees' environmental awareness.

EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. Equal employment opportunity, including veterans and individuals with disabilities.

PI283414296

General Requirements (Outer) Skills (Inner) Specialized (Center) 0% Occupation 0% Education 0% Work Experience 0% Location 0% Salary N/A Job Skills N/A Shift N/A Min. Age N/A Drivers Lic. N/A DL Endorsements N/A Typing N/A Security Clearance N/A Language This chart is used to compare your background against this job to help to determine if you would be a good fit for this position. You match 0% of the General Job Requirements. You match 0% of the Skills Required, and you match 0% of the Specialized Job Requirements. End of interactive chart. View Share Technical Writer Bachem Americas, Inc. Vista, CA Technical Writers Regular | $61,171.20-$84,110.40 Year Corporate - 1 week ago Technical Writer Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. A brief overview The Technical Writer I will prepare cGMP documentation, including protocols, reports, studies, Failure Mode and Effect Analyses (FMEAs), memos, forms, specifications, qualifications, change controls, deviations, Corrective and Preventative Actions (CAPA), Standard Operating Procedures (SOPs), and Master Batch Production Records (MBPRs). What you will do

• Write and revise documentation, such as protocols, reports, SOPs and associated forms, and MBPRs. Review and complete all documentation following cGMP guidelines
• Ensure collaboration between all applicable departments, such as Production, Facilities, Materials Management, QA and QC
• Adhere to manufacturing schedules and timelines
• Participate in the validation of products and processes
• Participate in project meetings with subject material experts General Requirements (Outer) Skills (Inner) Specialized (Center) 0% Occupation 0% Education 0% Work Experience 0% Location 0% Salary N/A Job Skills N/A Shift N/A Min.

Age N/A Drivers Lic. N/A DL Endorsements N/A Typing N/A Security Clearance N/A Language This chart is used to compare your background against this job to help to determine if you would be a good fit for this position. You match 0% of the General Job Requirements. You match 0% of the Skills Required, and you match 0% of the Specialized Job Requirements. End of interactive chart. View Share See all jobs from Bachem Americas, Inc. Location/Work Site Information Help for Location/Work Site Information. Opens a new window. Cost of Living Calculator Help for Cost of Living Calculator. Opens a new window. Compensation and Benefits Help for Compensation and Benefits. Opens a new window. Job Type and Required Hours Help for Job Type and Required Hours. Opens a new window. Work Experience Help for Work Experience. Opens a new window. Education and Training Help for Education and Training. Opens a new window. Skills Required Help for Skills Required. Opens a new window. Specialized Job Requirements Help for Specialized Job Requirements. Opens a new window. Occupation Information for Purchasing Managers Help for Occupation Information for Purchasing Managers. Opens a new window. Other Jobs and Employers Help for Jobs Available , opens a new window. Career Ladder Help for Career Ladder. Opens a new window. Personal Requirements Help for Personal Requirements. Opens a new window. Nature of the Work Help for Nature of the Work. Opens a new window. Work Values and Activities Help for Work Values and Activities. Opens a new window. Change Job Search Criteria Print Job Order Opens in new window [ Do you have a comment or concern about this job posting? ] About Sign In / Register Home Site Map Site Search Explore CalJOBS Settings Accessibility Statement Preferred Settings Page Preferences Languages Services For Individuals For Employers Labor Market Mobile App Legal Privacy Statement Terms of Use Disclaimer Equal Employment Opportunity Resources Protect Yourself Assistance CalJOBS Contact Us Statewide Sacramento, CA 94280 Copyright © 1998-2026 Geographic Solutions, Inc. All Rights Reserved. Virtual OneStop® - VOS Sapphire AI v24