Current jobs related to Deviations Investigator - Durham - DPS Group


  • Durham, North Carolina, United States Randstad Enterprise Full time

    Biomanufacturing Investigator OpportunityRandstad Enterprise is seeking a skilled Biomanufacturing Investigator to support Large-Scale Biomanufacturing operations. The ideal candidate will ensure thorough investigations and resolutions to minor deviations, collaborating cross-functionally to implement solutions and optimize operations.Main...


  • Durham, United States Randstad Enterprise Full time

    Randstad Enterprise is seeking an experienced Biomanufacturing Investigator to join the team! The Majors Investigator II will support Large-Scale Biomanufacturing to ensure thorough investigations and resolutions to minor deviations. Collaborating cross-functionally with positive end results and the implementation of solutions/CAPAs that optimize...


  • durham, United States Randstad Enterprise Full time

    Randstad Enterprise is seeking an experienced Biomanufacturing Investigator to join the team! The Majors Investigator II will support Large-Scale Biomanufacturing to ensure thorough investigations and resolutions to minor deviations. Collaborating cross-functionally with positive end results and the implementation of solutions/CAPAs that optimize...


  • Durham, United States Randstad Enterprise Full time

    Randstad Enterprise is seeking an experienced Biomanufacturing Investigator to join the team! The Majors Investigator II will support Large-Scale Biomanufacturing to ensure thorough investigations and resolutions to minor deviations. Collaborating cross-functionally with positive end results and the implementation of solutions/CAPAs that optimize...

  • QC Technical Writer

    4 weeks ago


    durham, United States MedPharm (formerly Tergus Pharma) Full time

    Support Laboratory Quality Systems including change control, investigations, deviations, events, SOP revisions, and documentation practices as part of the quality and compliance objectives.Conduct investigations related to quality systems such as deviations, events, NCRs, CAPAs, OOS, NOEs, complaints, and Quality Protocols of high complexity; works closely...

  • QC Technical Writer

    4 weeks ago


    durham, United States MedPharm (formerly Tergus Pharma) Full time

    Support Laboratory Quality Systems including change control, investigations, deviations, events, SOP revisions, and documentation practices as part of the quality and compliance objectives.Conduct investigations related to quality systems such as deviations, events, NCRs, CAPAs, OOS, NOEs, complaints, and Quality Protocols of high complexity; works closely...

  • Technical Writer

    4 months ago


    Durham, United States Tergus Pharma Full time

    Support Laboratory Quality Systems including change control, investigations, deviations, events, SOP revisions, and documentation practices as part of the quality and compliance objectives.Conduct investigations related to quality systems such as deviations, events, NCRs, CAPAs, OOS, NOEs, complaints, and Quality Protocols of high complexity; works closely...


  • Durham, North Carolina, United States Piper Companies Full time

    Piper Companies is currently in search of a Quality Assurance Specialist to become a part of a cell and gene therapy organization that is pioneering advanced AAV platform products aimed at addressing complex diseases. The Quality Assurance Specialist will play a crucial role in the evaluation and endorsement of data within a GMP setting. This position...


  • Durham, North Carolina, United States Piper Companies Full time

    Piper Companies is currently in search of a Quality Assurance Specialist to become part of a cell and gene therapy organization focused on developing groundbreaking AAV platform products aimed at addressing complex diseases. The Quality Assurance Specialist will play a crucial role in the evaluation and endorsement of data within a GMP framework. This...


  • Durham, North Carolina, United States KBI BioPharma Full time

    Job SummaryWe are seeking a highly skilled Senior Quality Assurance Specialist to join our team at KBI Biopharma. This role will be responsible for ensuring the quality and compliance of our manufacturing operations, collaborating with cross-functional teams to resolve production-related deviations and other compliance issues, and providing training and...

  • Sr. QA Specialist

    4 weeks ago


    Durham, United States BioCryst Pharmaceuticals Full time

    Description COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with complement-mediated and other rare diseases. For over three decades we've been guided by our passion for not settling for "ordinary" in our quest to develop novel medicines. We leverage our expertise in structure-guided drug design to develop...


  • Durham, North Carolina, United States KBI BioPharma Full time

    Job Title: Senior Manager Quality AssuranceThis role is responsible for providing QA oversight of the Deviations, CAPA, and Complaints organization. The Senior Manager works closely with the Program Management team to facilitate communications between KBI and clients regarding quality-related events.Key Responsibilities:Function as the system owner for the...


  • Durham, North Carolina, United States KBI BioPharma Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Specialist to join our team at KBI Biopharma. The successful candidate will be responsible for ensuring the quality and compliance of our products, collaborating with cross-functional teams, and mentoring junior QA staff.Key ResponsibilitiesCollaborate with Manufacturing, QA, and other departments...


  • Durham, North Carolina, United States Resilience Corp. Full time

    Job SummaryA career at Resilience is more than just a job - it's an opportunity to change the future. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.Job ResponsibilitiesEnsure manufacturing compliance with applicable procedures,...


  • Durham, North Carolina, United States CARsgen Therapeutics Full time

    Job SummaryWe are seeking a highly skilled Facilities Engineer II to join our team at CARsgen Therapeutics' Durham facility. As a key member of our Maintenance and Engineering department, you will play a critical role in ensuring the smooth operation of our GMP manufacturing facility.Key ResponsibilitiesMaintenance Coordination: Coordinate maintenance...


  • Durham, United States Piper Companies Full time

    Piper Life Sciences is actively seeking a Quality Assurance Specialist to join a cell &gene therapy organization developing innovative AAV platform products for challenging diseases. The Quality Assurance Specialist will be responsible for the review and approval of data in a GMP environment. This is a Monday - Friday, traditional hours role that is...


  • Durham, North Carolina, United States SpringWorks Therapeutics Full time

    Job Summary:We are seeking a highly motivated and experienced Quality Assurance professional to join our team at SpringWorks Therapeutics as a Quality Assurance Manager. This individual will play a critical role in ensuring the quality and compliance of our products, working closely with internal stakeholders and external partners to maintain a reliable and...


  • Durham, North Carolina, United States CARsgen Therapeutics Full time

    Job SummaryThe Quality Assurance Operations Specialist will be responsible for day-to-day support of Good Manufacturing Practice (GMP) operations at CARsgen Therapeutics' facility for clinical and commercial products.Key ResponsibilitiesQA Operations Support: Provide on-the-floor QA support for GMP operations, including in-process batch record review, QA...


  • Durham, United States CARsgen Therapeutics Full time

    Position Summary: The Quality Assurance (QA) Operations Specialist will be responsible for day-to-day support of GMP operations at the RTP CARsgen facility for clinical and commercial products. The team member will provide QA oversight of clinical trial drug production supporting raw material and product disposition. Additionally, this role is responsible...


  • Durham, United States CARsgen Therapeutics Full time

    Position Summary: The Quality Assurance (QA) Operations Specialist will be responsible for day-to-day support of GMP operations at the RTP CARsgen facility for clinical and commercial products. The team member will provide QA oversight of clinical trial drug production supporting raw material and product disposition. Additionally, this role is responsible...

Deviations Investigator

4 months ago


Durham, United States DPS Group Full time
Summary
DPS Group is seeking a Deviations Investigator for a client in Durham, NC. Successful candidates will lead, write, and review deviations and investigations for the client. This includes the manufacturing, facilities, supply chain/materials management and support QC deviations as necessary. This position is based onsite in Durham, NC.

Responsibilities
  • Lead, write and review deviations and investigations, including the manufacturing, facilities, supply chain/materials management and support QC deviations as necessary
  • Identify and assemble proper SMEs for triage, determine immediate actions taken, document impact assessments, lead RCA, develop appropriate CAPAs
  • Strong knowledge of cGMP requirements for manufacturing
  • Experience working in electronic Quality Management System
  • Demonstrated understanding of the principles and applications associated with cell and gene manufacturing operations, maintenance/calibration, engineering, and validation
  • Deliver On-Time Closure of Deviations to support Batch-On-Time-Delivery commitments for Tech Transfer - New Product Introduction, Clinical, and Commercial Products
  • Other duties as assigned

Skills and Qualifications
  • Bachelors or Advanced degree in a scientific discipline.
  • Experience in the pharmaceutical/biotech industry in combination with drug substance/drug product manufacture, development and/or quality.
  • Excellent verbal and written communication skills, detail-oriented personality, and ability to work collaboratively across functions.
  • Experience interacting with regulatory health authorities inspections.
  • Knowledge of global regulations and standards.
  • Strong team player that has a customer service approach and is solution oriented.
  • Attention to detail and the ability to work individually as well as within a multi-disciplinary team.
  • Excellent listening, communication and interpersonal skills fostering team spirit.
  • Consistent delivery of high-quality work at all times.
  • Ability to gown and work in a cleanroom environment.
  • Ability to provide legal US work authorization documents required. Will consider US domestic travelers and relocation.

Additional
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Continuous Learning -Assesses own strengths and weaknesses. Pursues training and development opportunities. Seeks feedback to improve performance. Shares expertise with others. Strives to continuously build knowledge and skills.
  • Culture - Supports a culture of excellence. Contributes to a collaborative environment that rewards teamwork, mentorship, best-in-practice development, and pride in workmanship.
  • Customer Services - Displays courtesy and sensitivity. Manages difficult or emotional customer situations. Meets commitments. Responds promptly to customer needs. Solicits customer feedback to improve service.
  • Planning and Organizing - Prioritizes and Plans work activities. Uses time efficiently. Plans for additional resources. Integrates changes smoothly, Sets goals and objectives. Works in an organized manner.
  • Teamwork - Balances team and individual responsibilities. Contributes to building a positive team spirit. Exhibits objectivity and openness to others' views. Gives and welcomes feedback. Puts success of team above own interests.
  • Use of Technology - Demonstrates required skills. Adapts to new technologies. Keeps technical skills up to date. Troubleshoots technological problems. Uses technology to increase productivity.
  • Language Ability - Read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Write routine reports and correspondence. Speak effectively before groups of customers or employees.
  • Mathematical Ability - Work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Apply concepts such as fractions, percentages, ratios and proportions to practical situations.
  • Reasoning Ability - Apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Deal with problems involving several concrete variables in standardized situations.

The Company
DPS Group is a global EPCMV firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries. DPS is dedicated to delivering successful projects with a 'client-first' mentality and personal touch across a range of market sectors: Project and Program Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification, and Start-up.

DPS Engineering Inc. is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. DPS does not discriminate in employment opportunities or practices on the basis of: race, color, religion, gender, national origin, age, sexual orientation, gender identity, disability, veteran status or any other characteristic protected by country, regional or local law.

#LI-KF1