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QA Area Specialist I - SDF (2nd shift)Merck & Co. • Durham, North Carolina, United States
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QA Area Specialist I - SDF (2nd shift)

Merck & Co.
  • US
    Durham, North Carolina, United States
  • US
    Durham, North Carolina, United States
Jetzt Bewerben

Über

About the Department For more than 100 years, Novo Nordisk has been tackling unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Being part of Novo Nordisk allows employees to help improve the quality of life for millions of people around the world.
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Emerging Technologies – Solid Dosage Forms US facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. SDF maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies.
What we offer you
Leading pay and annual performance bonus for all positions
All employees enjoy generous paid time off including
14 paid holidays
Health Insurance, Dental Insurance, Vision Insurance - effective day one
Guaranteed 8% 401K contribution plus individual company match option
Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
Free access to Novo Nordisk-marketed pharmaceutical products
Tuition Assistance
Life & Disability Insurance
Employee Referral Awards
The Position Ensure Batch Production Records (BPRs) and/or relevant quality processes are compliant with regulations and/or relevant standard operating procedures (SOPs) and guidance.
Accountable for Quality review & approval of Change Requests (CRs), Deviations & other documentation. Perform Self Audits (in conjunction with line of business (LoB)), Quality Assurance (QA) presence & process confirmation on shop floor.
Relationships Reports to Manager, Quality Assurance.
Essential Functions
Ensure site compliance with Regulations, International Organization for Standardization (ISO) standards, corporate & local SOPs
Review & approve documentation for Quality approval - batch records and other documentation
Support, review & approve investigations & root-cause analysis using LEAN tools and continuous improvement
Participate in process confirmations & Go Look Sees
Evaluate trend & report data for Quality Management Reviews (QMRs) & Annual Product Review (APR) reports
Perform QA role to review and approve local production related Customer Complaint Investigations (escalate if necessary)
Participate in & support the audit management team as needed during internal, external audits and inspections
Responsible for training of AP and FP members responsible for conducting investigations
Follow all safety & environmental requirements in the performance of duties
Other duties as assigned
Physical Requirements May move equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. May be required to be on your feet for up to a 12-hour shift. May required corrected vision to 20/20 or 20/25 based on role. May require color vision based on role. May require the ability to work in loud noise environments with hearing protections.
Qualifications
Associate's degree in life sciences or related field from an accredited college required. Bachelor's degree preferred
May consider a High School Diploma or GED with a minimum of six (6) years of experience in QA or related quality experience
Minimum of two (2) years QA and /or quality related, or API experience required, preferably in the pharmaceutical industry
Quality Experience preferred
General knowledge of pharmaceutical regulations & quality systems preferred
Knowledge of Quality and one or more of the following: Aseptic Production, Business Support, QC, Production Support, Warehousing/Transport, API, and/or Finished Production processes preferred
Excellent written & verbal communication skills required
Basic computer skills in MS Office, MS Project, PowerPoint, etc. required
Equal Opportunity Employment Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.
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  • Durham, North Carolina, United States

Sprachkenntnisse

  • English
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