Quality Assurance Tech II

Reposted 7 Days Ago
Be an Early Applicant
St. Louis, MO, USA
In-Office
1-3 Annually
Junior
Healthtech • Pharmaceutical • Telehealth
The Role
Ensure QA compliance through document review and inspection in a cGMP environment, addressing discrepancies and supporting manufacturing operations.
Summary Generated by Built In

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Job Description Summary

The Quality Assurance Technician II performs a variety of review processes with the intent to correct record errors in manufacturing process documentation that includes batch record review and documentation issue resolution. This role is also responsible for return good inspections, cGMP area inspections and product inspections. This role ensures QA compliance and that cGMP principles are adhered to.

Job Description

ESSENTIAL FUNCTIONS:

  • Execute batch record review and document deficiencies in a computerized system
  • Identify exceptions and report exceptions to production
  • Resolve documentation discrepancies and issues with manufacturing operations personnel in a timely manner to allow for material release
  • Perform batch record accountability and Iron Mountain box reconciliation
  • Execute line clearances and assist in inspection of returned goods
  • Follow all internal and basic cGMP guidelines for pharmaceutical operations
  • Perform GMP walkthroughs with production on a routine basis
  • Participate in cross-functional teams to improve review efficiency and support
  • Adhere to all safety rules and maintain 100% completion of all safety required training
  • Maintain 100% on time Compliance Wire training

MINIMUM REQUIREMENTS:

Education:

HS Diploma is required; Associates or Bachelor’s degree is preferred.

Experience:

  • Minimum of 1-3 years of document review experience in a cGMP environment preferred. 
  • Proficiency in MS Word and Excel. 
  • Proven knowledge of FDA and cGMP regulations preferred.
  • LIMS, BPCS, and TrackWise experience preferred.

Preferred Skills/Qualifications:

  • Ability to communicate at a high level of written and oral skills
  • Ability to read and comprehend complex calculations and formulas
  • Ability to focus and review batch records for an extended period of time
  • Knowledge of cGMPs for APIs
  • Ability to quickly identify, communicate and/or resolve issues
  • Ability to read and understand complex batch records
  • Ability to keep batch records organized and easily retrievable at all times
  • Excellent verbal and written communication skills
  • Ability to understand and apply good documentation practices
  • Ability to build relationships with partners

COMPETENCIES:

Organizing, Peer Relationships, Functional/Technical Skill, Time Management, Priority Setting, Attention to Detail

ORGANIZATIONAL RELATIONSHIP/SCOPE:

Reports to Quality Supervisor. Works with Manufacturing and Quality personnel on a daily basis

WORKING CONDITIONS:

  • 85 % Office environment which includes sitting for long periods of time and computer use.
  • 15 % Manufacturing environment exposure including temperature, noise, or chemical exposure.

DISCLAIMER:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills require

EEO Statement:

We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. 

Top Skills

Bpcs
Lims
Excel
Ms Word
Trackwise
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The Company
Montreal, Quebec
1,722 Employees
Year Founded: 1997

What We Do

At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs. Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward. Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life. Endo has global headquarters in Malvern, Pennsylvania. Community Guidelines: 1. Be respectful. Everyone who visits our page should feel comfortable and respected. 2. If we see a comment that violates anything in the following list, it may be removed. • Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional. • Comments that are excessively repetitive and/or disruptive to the community. • Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter. • Comments that appear to be medical advice. We reserve the right to remove a reply for any reason at any time. 3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088. Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.

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