Talent Program - Assoc. Spclst, Quality Assurance - Rotational Program

Job Description

Our Quality Assurance group ensures our products are manufactured, processed, tested, packaged, stored and distributed in alignment with our incredibly high standards of quality and meet all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.

The Quality Line Oversight Program at West Point is an entry level 2 year program with 8 month rotations focused on providing hands‑on experience in pharmaceutical quality assurance supporting our Company’s largest and most complex vaccine manufacturing plant site. This entry level program provides individuals with a range of experiences across several core quality functions fostering a foundational introduction to the vaccine manufacturing business.

Successful candidates will be part of the Quality Line Oversight Program as a Quality Associate Specialist located at the West Point, PA site.

• Quality checks of finished product including visual inspection of vials, syringes and packages
• Verification of appropriate line clearance between batches to prevent product mix‑ups
• GMP document / batch record review

• Rotational support of Quality Assurance, Quality Operations, and Environmental Monitoring providing a foundational understanding of vaccine quality oversight and production
• Continuous improvement projects by participating in problem solving and partnering with Operations, Technology, and other Quality groups in areas such as safety, quality, and efficiency

The shift structure for the position includes 12‑hour day and night shifts which rotate approximately every 9 weeks. The position does require weekend coverage. Both the initial assignment and future opportunities can include off‑shift/off‑schedule support within a vaccine manufacturing operations area.

• Bachelor’s Degree in Engineering or Sciences (minimum)
• 0‑2 years of experience in a cGMP pharmaceutical environment preferred; internships, co‑operative education or other roles acceptable for entry level

• Willing to work alternate shifts and weekends
• Ability to focus on and obtain results
• Good verbal and written communication skills
• Ability to effectively collaborate within and across an integrated manufacturing team
• Ability to enact conflict resolution
• Ability to effectively respond to change
• Excellent analytical and organizational skills
• High personal integrity, credibility and energy
• Flexibility to perform related tasks to support the business
• Computer literacy in MS Office, Word, Outlook, Excel

• 0‑2 years working experience in a cGMP pharmaceutical environment
• Experience using Lean/Six Sigma tools

$70,500.00 – $ (range based on factors such as education, experience, location, and business needs)

We offer a comprehensive package of benefits including medical, dental, vision, other insurance benefits for employee and family, retirement benefits including 401(k), paid holidays, vacation, and compassionate and sick days. More information at

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.

For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit.

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U.S. Hybrid Work Model:
Effective September 5, 2023, employees in…