Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

QA Associate- Micro Reviewer

RK Pharma Inc

About RK Pharma RK Pharma is a pharmaceutical organization dedicated to delivering high-quality, affordable drug products through disciplined execution and strong internal collaboration. Our work is not patient-facing, but it directly supports the safety, reliability, and compliance of products relied upon downstream. Description We value people who take pride in careful work, respect quality systems, and understand that consistency and sound judgment matter more than speed or spotlight. About the Role The QA Associate – Microbiology supports microbiology‑related quality activities to ensure processes, data, and documentation meet GMP and regulatory expectations. This role works closely with Microbiology, Manufacturing, and other Quality functions to help maintain a state of control across facilities and systems. This position is well‑suited for someone with a microbiology background who is detail‑oriented, thoughtful, and comfortable working within structured quality systems. Success comes from steady judgment, clear communication, and the confidence to ask questions or raise concerns when something does not look right. Key Responsibilities Provide Quality Assurance support and oversight for microbiology‑related activities, including environmental monitoring and utility monitoring. Review microbiology data, records, and reports for accuracy, completeness, and GMP compliance. Support investigations related to microbial excursions, deviations, and OOS/OOT results; assist with CAPAs, change controls, and risk assessments that impact microbiology systems. Ensure documentation is completed clearly, accurately, and in accordance with approved procedures. Participate in internal audits, inspections, and readiness activities as needed. Collaborate with Microbiology, Manufacturing, Validation, and broader Quality teams. Escalate quality concerns promptly and appropriately through established channels. Required Qualifications Bachelor’s degree in Microbiology, Biology, or a related scientific discipline. Experience in a GMP‑regulated pharmaceutical, biotechnology, or similar environment. Working knowledge of microbiology concepts such as environmental monitoring, contamination control, and aseptic practices. Strong attention to detail and disciplined documentation habits. Ability to follow established procedures and quality systems. Clear written and verbal communication skills. Preferred Qualifications Prior experience in Quality Assurance or QC Microbiology. Familiarity with cleanroom operations and environmental monitoring programs. Experience supporting audits or regulatory inspections. How We Work At RK Pharma, quality takes priority over speed. Procedures are followed for a reason. Questions and escalation are encouraged. Helpfulness and respect are expected across teams. No one is asked to cut corners to meet a deadline. People who do well here are steady, thoughtful, and comfortable letting the quality of their work speak for itself. Physical and Work Environment Ability to work in controlled environments, including cleanrooms as required. Ability to review data and documentation for extended periods. Compliance with gowning, hygiene, and safety requirements. What We Offer A stable, quality‑focused work environment. Clear expectations and structured onboarding. Collaboration with experienced Quality and Microbiology professionals. The opportunity to directly support product quality and compliance. Equal Opportunity Employer RK Pharma is an equal opportunity employer. We are committed to fair, consistent, and respectful hiring practices. #J-18808-Ljbffr

Vacancy posted 10 hours ago
Similar jobs that could be interesting for youBased on the QA Associate- Micro Reviewer in Pearl River, NY vacancy
  •  ...QA Associate The QA Associate supports the site's Quality Management System by managing product complaints, adverse events, and investigation...  .... Trend reports will be developed with the year in review of data, to drive and address areas subject to continuous improvement... 
    Suggested
    Work at office
    Shift work

    Strides Pharma Inc.

    Spring Valley, NY
    4 days ago
  • $30 - $35 per hour

     ...thru 4:00pm Manager Notes: ~ High School diploma 5 years Degree, 3 + years of experience Bachelor's degree, final batch review 1+ year of experience Must Have: Experience; CAPA, Batch review, technical writing, knowing how use documentation... 
    Suggested
    Monday to Friday
    Shift work

    Integrated Resources

    Pearl River, NY
    1 day ago
  • $18.75 per hour

    At Iron Mountain we know that work, when done well, makes a positive impact for our customers, our employees, and our planet. That’s why we need smart, committed people to join us. Whether you’re looking to start your career or make a change, talk to us and see how you...
    Suggested
    Monday to Friday
    Shift work

    Iron Mountain Inc

    Valley Cottage, NY
    10 hours ago
  •  ...Work Schedule Monday thru Friday; 7:30am thru 4:00pm Responsibilities Track and review manufacturing batch records to ensure compliance with regulatory requirements. Follow up with Manufacturing Technicians to ensure corrections are completed in a timely manner. Maintain... 
    Suggested
    Monday to Friday

    Merck & Co. Inc

    Pearl River, NY
    4 days ago
  •  ...Job Title Work Schedule: Monday thru Friday; 7:30am thru 4:00pm 1st Shift: Track and review manufacturing batch records to ensure compliance with regulatory requirements. Follows up with Manufacturing Technicians to ensure corrections are completed in a timely manner... 
    Suggested
    Monday to Friday
    Day shift

    Aequor Inc

    Pearl River, NY
    3 days ago
  • $35.46 per hour

     ...Adecco Healthcare & Life Sciences Batch Record Reviewer / Quality Documentation Specialist Fully Onsite | 1st Shift | Temp Role...  ...High School Diploma with 5+ years of relevant experience, OR Associate Degree with 3+ years of experience, OR Bachelor's Degree... 
    Hourly pay
    Temporary work
    Casual work
    Local area
    Monday to Friday
    Day shift

    Adecco Colombia S.A.

    Pearl River, NY
    4 days ago
  • $18.75 per hour

    Document Imaging Specialist Iron Mountain is seeking a detail-oriented Document Imaging Specialist to join our Digital Solutions team. In this role, you will be responsible for converting physical records into high-quality digital assets while maintaining strict production...
    Monday to Friday
    Shift work

    Iron Mountain Incorporated

    Orangeburg, NY
    10 hours ago
  • RK Pharma Inc is seeking a QA Associate in Microbiology in Pearl River, NY. This role involves providing quality assurance support for...  ...meet GMP and regulatory standards. Responsibilities include reviewing microbiology data, supporting investigations, and participating... 

    RK Pharma Inc

    Pearl River, NY
    1 day ago
  • Eacademy Sanofi is looking for a Quality Assurance Specialist in Pearl River, NY. You will provide direct support to ensure compliance with Good Manufacturing Practices (GMP) and manage quality-related issues on the shop floor. The ideal candidate has a Bachelor's degree...

    Eacademy Sanofi

    Pearl River, NY
    2 days ago
  • Sanofi is looking for a Quality Assurance Specialist in Pearl River, NY. This role involves ensuring compliance with Good Manufacturing Practices (GMP) and supporting quality management activities on the shop floor. The ideal candidate will have a bachelor’s degree and...

    Sanofi

    Pearl River, NY
    1 day ago
  •  ...biopharmaceutical company in New Jersey is seeking an experienced Quality Assurance Associate III. The role involves providing comprehensive QA oversight for manufacturing operations, reviewing deviations and approvals in compliance with FDA cGMP standards. Ideal candidates... 
    Full time

    Medix

    Allendale, NJ
    10 hours ago
  • $90k - $110k

     ...Document Lifecycle Management and Quality Assurance: Manage the full document lifecycle from receipt and submission through review, approval, distribution, and final archiving. Facilitate the review and approval of all Project documents, drawings, and specifications... 
    Full time
    For subcontractor
    Flexible hours

    Veolia | France

    Haworth, NJ
    2 days ago
  •  ...initiatives to promote a quality-focused culture (A) About You Bachelor's degree with minimum 2 years of quality assurance experience, OR associate degree with 3+ years of quality assurance experience. Comprehensive knowledge of Good Manufacturing Practices (GMP) and quality... 

    Eacademy Sanofi

    Pearl River, NY
    3 days ago
  • $90k - $110k

    Document Controller The Document Controller is responsible for managing the entire lifecycle of documentation and information flow within a construction project. This critical role ensures the accuracy, integrity, traceability, and accessibility of all project-related ...
    Full time
    Flexible hours

    Sarpi Thinktech

    Haworth, NJ
    4 days ago
  • $90k - $110k

    Veolia is seeking a Document Controller in Haworth, NJ, who will be responsible for managing documentation and information flow within a construction project. This is a full-time onsite role requiring strong attention to detail and organizational skills, with a salary ...
    Full time

    Veolia

    Haworth, NJ
    4 days ago
  • $90k - $110k

    Sarpi Thinktech is seeking a Document Controller to manage the entire lifecycle of documentation at the Haworth Water Treatment Plant. This full-time position requires 5+ years of experience in document management, particularly on major projects, and proficiency in systems...
    Full time

    Sarpi Thinktech

    Haworth, NJ
    4 days ago
  •  ...Description Job Description Position summary The Quality Associate I, Operations is responsible for actively participating in “on...  ...Participates as a team member on cross-functional teams. Participates in reviews and structured processes for continuous improvement Roles... 
    Shift work

    Strides Pharma Inc

    Spring Valley, NY
    5 days ago
  • Veolia NA is seeking a Document Controller for their Haworth Water Treatment Plant in New Jersey. This full-time position focuses on managing document control processes, ensuring compliance, and providing training to project teams. The ideal candidate should have a Bachelor...
    Full time

    Veolia NA

    Haworth, NJ
    3 days ago
  • $45 - $55 per hour

     ...Documentation Practices. Identify and implement improvement opportunities to increase the efficiency and effectiveness of the QMS and associated documentation. Required Education, Work Experience & Related Competencies BS in a science, engineering, business or related... 
    Work experience placement
    Immediate start

    Kelly Science, Engineering, Technology & Telecom

    Mahwah, NJ
    3 days ago
  • $60k - $67k

    LEGAL ADMINISTRATIVE ASSISTANT (DP SPECIALIST) Archer & Greiner, P.C. seeks a full-time Legal Administrative Assistant (DP Specialist) to work in its Hackensack, NJ office. Hours are Monday through Friday, 9:00 AM to 5:00 PM. At Archer, we are passionate about developing...
    Full time
    Temporary work
    Work at office
    Monday to Friday

    Archer & Greiner, P.C.

    Hackensack, NJ
    4 days ago
  • Engineering process documentation specialist position for a manufacturing company. The focus is on improving the engineering documentation process, and is not manufacturing or production focused. Primary responsibilities will include:. Responsible for engineering process...

    Engineering-Resource-Group

    Ramsey, NJ
    5 days ago
  • Engineering-Resource-Group, located in Ramsey, New Jersey, is seeking a specialist in engineering process documentation. The focus will be on improving engineering documentation processes, ensuring clarity and structure, and enhancing workflow standardization. The ideal...

    Engineering-Resource-Group

    Ramsey, NJ
    10 hours ago
  • $85k - $105k

    We are seeking an experienced Process Engineer to own and improve internal processes across product development and operations. This role will focus on building, documenting, and optimizing workflows to ensure efficiency, consistency, and scalability across teams. Responsibilities...

    Chefman

    Mahwah, NJ
    4 days ago
  • Engineering-Resource-Group is offering a permanent position for a Quality Technician / Quality Inspector based in Pearl River, New York. The role involves performing detailed SMT and PCB inspection to ensure compliance with established specifications. The ideal candidate...
    Permanent employment

    Engineering-Resource-Group

    Pearl River, NY
    2 days ago
  •  ...Scientific Recruiter focusing in NJ, PA, and DE Quality Assurance Associate II – Allendale, NJ Our vision is creating future cell therapy...  ...procedures. Key responsibilities include document management, review of manufacturing batch records, quality control (QC) data, facilitating... 
    Full time
    Contract work
    Work at office

    ClinLab Staffing

    Allendale, NJ
    4 days ago
  • Jawonio is seeking a Quality Assurance Specialist in New City, NY. This full-time position involves developing quality assurance strategies to enhance compliance within the Corporate Compliance/Quality Assurance Department. The successful candidate will conduct audits,...
    Full time

    Jawonio

    New City, NY
    4 days ago
  • Quality Assurance Specialist Ready to proactively identify problems with products and goods? In manufacturing and industrial environments, that's what quality assurance specialists and technicians do best. If you have what it takes to report and verify defects, troubleshoot...
    Immediate start

    Randstad

    Sloatsburg, NY
    6 days ago
  •  ...regulatory requirements. The role involves inspecting components, reviewing documentation, and approving parts for service. No prior...  ...attention to detail is essential. The ideal candidate will have an Associate degree, the ability to follow precise instructions, and be... 
    Afternoon shift

    Chromalloy

    Orangeburg, NY
    4 days ago
  •  ...is important to product safety. It focuses on verifying work, reviewing paperwork, and making sure procedures are followed. No prior quality...  ...work schedule will be Tuesday - Saturday Requirements Associate degree or equivalent Company authorization to perform inspections... 
    Permanent employment
    Flexible hours
    Afternoon shift

    Chromalloy

    Orangeburg, NY
    10 hours ago
  • Orange & Rockland is seeking a Senior Specialist in West Nyack, New York. This role focuses on analyzing and coordinating Department activities, procurement efforts, and compliance programs. The ideal candidate must have strong communication skills and a Bachelor's Degree...

    Orange & Rockland

    West Nyack, NY
    4 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to QA Associate- Micro Reviewer. Be the first to apply!