Science/Pharma/Food jobs

Browse our selection of 129 Science/Pharma/Food jobs below or use advanced job search to refine or expand the results.

  • ORION GROUP
    PRODUCT QUALITY SPECIALIST
    ORION GROUP
    DUBLIN
  • SIGMAR RECRUITMENT
    QC ANALYST
    SIGMAR RECRUITMENT
    CORK
  • CAREERWISE RECRUITMENT
    TECHNICIAL TRANSFER LEAD
    CAREERWISE RECRUITMENT
    DUBLIN
  • CAREERWISE RECRUITMENT
    DIRECTOR (CLINICAL TRIALS)
    CAREERWISE RECRUITMENT
    CORK
  • CPL
    REGULATORY AFFAIRS TEAM LEAD SUBMISSIONS
    CPL
    DUBLIN WEST
  • CPL
    QUALITY ASSURANCE MANAGER
    CPL
    DUBLIN CITY CENTRE
  • CAREERWISE RECRUITMENT
    SCIENTIST
    CAREERWISE RECRUITMENT
    LIMERICK
  • ORION GROUP
    SENIOR QA SPECIALIST
    ORION GROUP
    DUBLIN
  • SIGMAR RECRUITMENT
    RAW MATERIALS MANAGER
    SIGMAR RECRUITMENT
    DUBLIN CITY CENTRE
  • CPL
    MEDICAL/SCIENTIFIC LIAISON (MSL)
    CPL
    DUBLIN WEST
PRODUCT QUALITY SPECIALIST
Posted on:
22/01/2020
Location:
DUBLIN
Salary:
NEGOTIABLE
Job type:
CONTRACT
Job reference number:
15486250
Client ID:
929546
Orion Group Sciences are looking for a Product Quality Specialist for our Multinational Pharmaceutical client based in the South of Dublin area on an initial 12-month contract with the potential to extend.


Job Purpose

As a Specialist Stability you will provide support to the Product Quality (PQ) organization as a subject matter expert of clinical and commercial product stability studies and GMP data management. In this team-based role, you will directly add to the success of a Product Quality Team by collaborating with diverse functional areas including Supply Chain, Manufacturing, Quality Control, Regulatory, Quality Assurance, Quality Engineering, International Quality and Process Development on projects, issue resolution and investigations.


Main Responsibilities of the role

  • Builds and monitors stability studies within quality systems (e.g. LIMS)
  • Owns and handles product quality and stability data and may serve as a primary author on regulatory filings and directly participate in and support site-based GMP inspections
  • Business process support, such as SOP authoring and management, or gap assessments to regional regulations
  • Build and maintain technical GMP documents and product stability studies
  • Review, verify, report, and archive GMP data for clinical and commercial products
  • Apply keen attention to detail to conduct data review and reports
  • Execute transactions in relevant GMP computer-based systems (change control, LIMS, etc.)
  • Adeptly manage time-sensitive activities independently

Desired Experience and Background of the successful candidate

  • Doctorate degree, or Master's degree
  • 3 years of Quality, Operations, Scientific, or Manufacturing experience
  • Or Bachelor's degree & 5 years of Quality, Operations, Scientific, or Manufacturing experience
  • Preferred Qualifications: B.S. or advance degree in chemistry, biochemistry, biology, or a related pharmaceutical sciences field and experience with growing responsibility in a quality, analytical development, process development, pharmaceutics, regulatory, or manufacturing environment
  • Expertise in project management, time management and successfully navigation skills for matrixed team environments are essential
  • Experience working in a regulated environment (either direct GMP or technical support)
  • Strong project management skills
  • Understanding of biologic and synthetic pharmaceutical bulk and drug product manufacturing and analytical techniques
  • General knowledge of cGMP and US and international filing regulations pertaining to the manufacture and testing of pharmaceuticals and/or bio-pharmaceuticals
  • Experience working on a cross-functional team in a matrix environment
  • Excellent written and verbal communication skills, including facilitation and presentation skills
#pharma #medical #bioassay #multinational #product #quality #LIMS #productstability #GMP #Pharmaceutical



For more information on this role, call Kate O' Sullivan on 44 (0) 2039 944702 or email Kate.OSullivan@orioneng.com for a completely confidential chat about this role and other opportunities using the reference number: 929546

Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.