18 days old

Quality Control Scientist III, Laboratory Support

Pfizer
Andover, MA 01810
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**ROLE SUMMARY**

Pfizer is seeking a talented individual to join our Quality Control Analytical (QCA) or Quality Control Raw Material (QC RM) team in Andover, MA. As an experienced member of the Quality organization, you will work outside the lab providing technical and documentation support, oversight of testing and scheduling and troubleshooting support. You will also serve as a backup to the lab manager. You will be assigned a primary lab/product of focus, but may flex to support other areas, as needed. Products include: plasmid DNA, vaccines, mAbs, proteins and raw materials.



If you have experience working in a Quality Control laboratory, have strong technical writing and troubleshooting skills, and want to support a lab from a non-testing perspective, then this position may be for you.



**ROLE RESPONSIBILITIES**

As a Quality Control Scientist III, Laboratory Support, you will provide non-testing support for your assigned lab/product. You will:



+ Support lab testing including assisting with assay troubleshooting, tracking testing and timelines, and reviewing data and documents for compliance and accuracy.

+ Maintain cGMP compliance and laboratory inspection readiness.

+ Provide audit support for board of health inspections and regulatory responses.

+ Drive and provide technical expertise for investigations, technical documents, test methods and Annual Product Quality Reviews (APQRs).

+ Support change controls, audits and commitments.

+ Provide back up support for the lab manager.

+ Identify, drive and participate in continuous improvement activities.

+ Participate in cross-functional teams.



The successful candidate will be a proven QC Scientist with deep laboratory experience, strong technical writing skills, ability to convey technical concepts to others, have a passion for continuous improvement, and enjoy providing subject matter expertise and support to fellow colleagues.



**BASIC QUALIFICATIONS**



+ Bachelor's Degree in Biology, Chemistry or related discipline required.

+ 3-5 years of applicable laboratory experience required.

+ Knowledge of analytical techniques include HPLC, Capillary Gel Electrophoresis, Peptide mapping and UV Spectrophotometry.

+ Extensive knowledge and practical application of relevant analytical testing and troubleshooting.

+ Strong technical writing skills, including investigations.

+ Experience with cGMPs, regulatory guidance and audits.

+ Demonstrated leadership skills in decision making, planning, and prioritization with a focus on team success in meeting defined metrics and timelines.

+ Strong troubleshooting skills.

+ Self-motivated and able to adapt to rapidly changing project priorities.



**PREFERRED QUALIFICATIONS**



+ Knowledge in ELISA and Bioanalytical method preferred.

+ Project management skills.

+ Experience with continuous improvement tools including standard work, visual management, and DMAIC.



**PHYSICAL/MENTAL REQUIREMENTS**



+ Normal lifting, sitting, standing and walking requirements to facilitate support of staff in the office and on the floor (laboratory, suites, etc.).



**NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS**



+ Position is first shift Monday through Friday. Some off hour (night/weekend/holiday) support may be required to support staff and operations.



**Other Job Details:**



+ Eligible for Relocation Package

+ Eligible for Employee Referral Bonus

+ \#LI-PFE



**Sunshine Act**

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.



**EEO & Employment Eligibility**

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.



Quality Assurance and Control
Posted: 2020-11-09 Expires: 2020-12-19
Sponsored by:
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Quality Control Scientist III, Laboratory Support

Pfizer
Andover, MA 01810

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