Food Safety Quality Specialist - Union City

Only for registered members Union City, United States

4 weeks ago

Default job background

Job summary

A key player in monitoring,
supporting and ensuring the compliance of food safety and quality requirements daily,
leading by example in Good Manufacturing Practices (GMP) for others,
working cohesively as a team to drive the improvement of food safety and quality.


Lorem ipsum dolor sit amet
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.

Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.

Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Get full access

Access all high-level positions and get the job of your dreams.



Similar jobs

  • Only for registered members Linden, NJ

    We are currently hiring within our Quality Team for a Quality Specialist. This role is ideal for a recent graduate who is looking to build a career in the food manufacturing industry. · Print and ensure the accuracy of the printed information on finished good labels and Certifica ...

  • Only for registered members Rahway

    The Quality Specialist will be responsible for serving as the quality representative for and providing quality oversight of contractors performing various GMP activities supporting the production of clinical supplies, on behalf of our Company. · ...

  • Only for registered members Rahway

    This Quality Specialist position involves batch documentation review to ensure compliance with current Good Manufacturing Practices (cGMPs) regulations and relevant regulatory filing submissions. Key responsibilities include evaluating and disposing of clinical supply materials, ...

  • Only for registered members Newark

    The primary purpose of the Quality Improvement Specialist position is to assist in the development and implementation of the University Hospital Quality Improvement Program. · BSN Registered Nurse with a license to practice in the State of New Jersey required. · Four (4) years of ...

  • Only for registered members Jersey City, NJ

    +This QA Specialist will collaborate with Purchasing, R&D, and other departments to maintain compliance standards, support audits. · + ...

  • Only for registered members Newark

    We believe that work is more than a place you go every day. It is about being inspired and motivated to achieve extraordinary things. · ...

  • Only for registered members Summit $30.45 - $34.45 (USD)

    This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. · ...

  • Only for registered members Summit $30.45 - $34.45 (USD)

    +This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. · +Requires bachelors degree in Science or related discipline. · Minimum 3-5 years of experience working in a regulated GxP environment. · ...

  • Only for registered members Summit $30.45 - $34.45 (USD)

    This position will support QA oversight of CTLs for CTO Vector External Manufacturing operations. · This role is accountable for oversight of routine Quality responsibilities related to outsourced testing · Deviationss CAPAs Change Controls Certificate of Analysis/Certificate of ...

  • Only for registered members Newark NJ , US

    We're looking for someone who takes pride in precision, thrives in structured environments, and enjoys ensuring that systems and processes perform exactly as intended. · Competitive hourly pay with additional performance incentives · ...

  • Only for registered members Summit

    The Global Supplier Quality, External QC - Vector will process external deviation and change records from our Contract Test Laboratories (CTL). Other duties may include; Coordinate shipping and testing of samples for lot release, PPQ, · PSQ and will compile vendor documentation t ...

  • Only for registered members Summit, NJ

    This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. external from our CTLs. · This role is accountable for oversight of routine Quality responsibilities related to outsourced testing, Deviati ...

  • Only for registered members Jersey City

    This is a direct hire opportunity where you will play a key role in ensuring food safety, regulatory compliance, and product quality. · ...

  • Only for registered members Murray Hill

    The Quality Specialist will coordinate the review, investigation, and corrective actions associated with product complaints with the responsible manufacturing facilities in accordance with Corporate and Divisional policies and procedures. · ...

  • Only for registered members Rahway $106,200 - $167,200 (USD)

    The Senior Specialist, Global Development Quality Operations is responsible for independent approval of documentation to support GMP clinical supply drug product manufacture testing release and maintenance. · This person will also independently approve documentation accompanying ...

  • Only for registered members Rahway Full time $106,200 - $167,200 (USD)

    The Senior Specialist Quality Assurance role involves independent approval of documentation for GMP clinical supply drug product manufacture, testing, release, and maintenance. This includes reviewing batch documentation, data, information procedures equipment systems facilities ...

  • Only for registered members Rahway, NJ

    The Rahway based Senior Specialist, Global Development Quality Operations, is responsible for independent approval of documentation to support GMP clinical supply drug product manufacture, · testing, release, and maintenance in support of our company's clinical supply programs.Ad ...

  • Only for registered members Staten Island, NY

    The QA Specialist will provide agency leadership with essential support in the areas of risk management and continuous quality improvement through activities such as internal audits and checks, review of external audits & audit responses, site visits, interviews with staff and in ...

  • Only for registered members Summit

    The R&D Quality Specialist is responsible for administration of integrated and comprehensive quality systems and controls that are appropriate, effective, efficient and continuously improving in order to ensure that R&D functions are operating in full compliance with sound scient ...

  • Only for registered members Jersey City

    We are seeking a highly organized and detail-oriented Installation Quality Specialist to support our North America operations. · ...

  • Only for registered members Summit

    Job summary:The Quality Assurance eSystem Specialists primary responsibility is to help assure the quality, integrity, and compliance of site Information Technology (IT) systems, · and maintain alignment between business process owners, end users, and other cross functional areas ...