Find & Apply For Program Manager Jobs in Woodway, Texas

Between $96k and

$184k

Per Year DOE (Depends on Experience)

Position range in McLennan County $70k - $148k Per Year Aseptic Process Simulation Program Coordinator

ABBVIE INC

Occupation:

Clinical Research Coordinators

Location:

Woodway, TX - 76712

Job Type:

Regular, Full Time (30 Hours or More), Permanent Employment, Other, see job description Shift

Posted:

10/02/2026

Positions available: 1

Source:

WorkInTexas

Web Site:

WorkInTexas

Onsite /

Remote:

Work onsite all of the time

Updated:

10/05/2026

Expires:

11/01/2026

Job #: 17076559

Job Requirements and Properties

Help for Job Requirements and Properties. Work Onsite

Full Time Education

Bachelor's Degree Experience

60 Month(s) Schedule

Full Time Job Type

Regular Duration

Permanent Employment Public Transit

Available Benefits Help for . The APS/Media Fill Program Lead for a sterile ophthalmic manufacturing site in Waco, TX, leads the site-wide program in alignment with current

GMP, FDA, EU

Annex 1, and AbbVie quality standards, developing and executing the annual strategy, overseeing protocols and documentation, coordinating cross-functional execution, and serving as the subject matter expert for investigations and inspection readiness.[1][2]The role also covers trend analysis, personnel qualification integration, CAPA and continuous improvement, regulatory and customer-audit support, technical leadership, mentorship, and monitoring industry and regulatory developments to strengthen contamination control and aseptic operations For anAseptic Process Simulation (Media Fill) Program Leadsupporting a sterile ophthalmic manufacturing site in Waco, TX, the responsibilities could include: Key Responsibilities Lead the site-wide Aseptic Process Simulation (APS/Media Fill) program to ensure compliance with current

GMP, FDA, EU

Annex 1, and AbbVie quality standards for sterile eye care manufacturing.

Develop, maintain, and the annual media fill strategy, including routine, validation, and intervention-based process simulations.

Serve as the subject matter expert (SME) for aseptic process simulation design, execution, investigation, and regulatory inspection readiness.

Collaborate with Manufacturing, Quality Assurance, Microbiology, Engineering, and Validation teams to ensure media fills accurately represent routine and worst-case manufacturing conditions.

Author, review, and approve APS protocols, risk assessments, reports, and associated quality system documentation.

Lead investigations, root cause analyses, and corrective and preventive actions (CAPA) related to media fill failures or atypical events.

Analyze APS performance metrics and trends to identify opportunities for continuous improvement and enhanced contamination control.

Ensure personnel qualification and requalification programs are effectively integrated with media fill requirements and aseptic practices.

Support regulatory inspections and customer audits by presenting APS program strategies, results, investigations, and compliance initiatives.

Drive continuous improvement initiatives related to contamination control, aseptic processing, and sterile manufacturing operations. Preferred Leadership Focus Provide technical leadership and mentorship for cross-functional teams involved in sterile manufacturing and contamination control.

Champion a culture of quality, compliance, and operational excellence across aseptic processing operations.

Monitor industry trends, regulatory expectations, and emerging best practices to continuously strengthen the site's APS program. Qualifications Bachelors degree in science or technical field. MBA degree is beneficial and preferred.

5-10 years of experience in areas such as supply chain, customer service, manufacturing, engineering, and project management. Broad business perspective, knowledge and understanding of manufacturing processes. Strong project experience and an ability to influence others are essential.

Strong Strategy development and planning skills coupled with necessary knowledge of pharmaceutical manufacturing and supply activities. Strong issue identification and problem analysis, with the ability to create and solutions based on the gathered data.

Proficiency with common program management communication software tools and techniques.

Knowledge of business financial systems and tools.

Collaborative approach in working with different teams and stakeholders in a globally oriented work environment

Proven leadership ability with excellent communication skills including listening, verbal presentation and written. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law: The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.

Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemay ultimately pay more or less than the posted range. This range may bemodified in thefuture. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees. This job is eligible toparticipate in our short-term incentiveprograms.

Note:

No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.

Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremains in the Company'ssoleandabsolutediscretion unless and until paid andmay bemodified at the Companys sole and absolute discretion, consistent withapplicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html Recruitment Fraud Alert We have recently become aware of various recruitment phishing scams targeting job seekers.

Please be advised:

AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.

If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks. If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, pleasecontact usimmediately. Protect yourself by verifying job offers and communications. Your safety is important to us.

Pay Range:

$ 96500 - 183500 USD Where We Work Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely

•, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.