Quality Control Analyst I Position Available In Broward, Florida

Quality Control Analyst I#25-61079
$0.00-$33.50 per hour
Sunrise, FL
All On-site Job Description
Our Client, a Pharmaceuticals company, is looking for a Quality Control Analyst I for their Sunrise, FL location.

Responsibilities:

This position performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records.
All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.
Carries out responsibilities in accordance with the organization’s policies, procedures, and state, Federal and local laws.
Complies with all safety rules and regulations.
Perform analysis on raw materials, finish goods, API, and control substances
Ensures that balances are reviewed and calibrated.
Perform peer review of laboratory testing as required.
Responsible for Wet Chemistry testing (such as LOD, PH, titration, etc.)
Work within a team to meet productions, validation, stability, and request deadlines.
Participates in troubleshooting of analytical test methods and laboratory instruments.
Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), and Standard
Operating Procedures (SOP’s) instructions.
Responsible for performing additional related duties as assigned.

Requirements:

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.
Requires a Bachelor’s degree, preferably in Chemistry or Microbiology, or equivalent education/experience with a minimum of two years relevant progressive experience in a Quality Control Laboratory environment.
Requires working knowledge of cGMP, DEA and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
Labware LIMS and/or Empower preferred experience preferred.
Microbiology testing experience preferred.
Solid understanding of the principles of analytical chemistry as it applies to HPLC, GC, FTIR, UV-Vis and other general analytical techniques.
Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management
Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, Trackwise and Qdocs.
Ability to effectively communicate scientific and/or technical ideas in writing.
Ability to communicate effectively with excellent written and oral communication skills.
Ability to interact positively and collaborate with co-workers, management and other internal stakeholders.
Self-directed with ability to organize and prioritize work.
Detail oriented with the ability to identify errors and/or inconsistencies while performing tasks.
Business, scientific and personal computer hardware and software applications.
Skill levels in MS Office including proficiency in Word, PowerPoint, Excel and SharePoint.
Must be able to maintain the highest levels of confidentiality, integrity and discretion.
Excellent verbal, written, and interpersonal skills required.
Works on problems of moderate scope where evaluation of contributing factors requires analysis of situation or data.
Exercises judgment within broadly defined practices and policies and selects methods and techniques for obtaining solutions.
Selects methods, techniques, and evaluation criteria for obtaining results.
Acts independently and proactively to recommend methods and procedures for problem resolution.
Able to identify solutions to general problems through collaboration and creativity.
Sitting for extended periods at workstation or mobile equipment.
Standing for extended periods at workstation or equipment.
Using fingers to perform activities such as picking, pinching or typing.
In accordance with the Americans with Disabilities Act, it is possible that requirements may be modified to reasonably accommodate disabled individuals. However, no accommodations will be made which may pose serious health or safety risks to the employee or others or which impose an undue hardship on the Company.
The requirements and responsibilities in this position description do not create an employment contract and are not meant to be all-inclusive. The incumbent is responsible to ensure compliance with all laws, regulations, codes, standards and company policies relevant to this position. This document in no way states or implies that only the duties described above are to be performed by the incumbent. The incumbent will be expected to follow instructions and perform duties as required by his or her supervisor and understand that aspects of their position may be changed by the Company on an as-needed basis. Why Should You Apply?
Health Benefits
Referral Program
Excellent growth and advancement opportunities As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.