Manager Quality Assurance Operations (m/f/d)

Sandoz

Marschall

Hybrid

EUR 604,000 - 1,122,000

Full time

4 days ago
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Job summary

Sandoz seeks a Manager Quality Assurance Operations to oversee QA projects, develop and review GMP documentation, and ensure compliance with cGMP standards. This role supports policies, improves QA processes, and coordinates audits and inspections.

Key duties include batch release coordination, deviation/complaint handling, pest-control oversight, and QA data management in SAP. Strong German and English, plus a scientific or technical BS, are required.

Qualifications

  • Basic degree in scientific, technical or relevant discipline.
  • BS or equivalent education/experience required.
  • Good knowledge of cGMPs and regulatory guidelines.
  • Strong organizational skills and attention to detail.

Responsibilities

  • Manage portfolio of QA projects and provide functional expertise.
  • Create and review GMP documents such as batch records and SOPs.
  • Clarify deficiencies in GMP documents with stakeholders.
  • Support internal policies and global compliance initiatives.
  • Develop and improve GMP processes to meet guidelines.
  • Coordinate Pest Control tasks and supervise external partners.
  • Prepare reports and risk assessments for area of responsibility.
  • Ensure compliance with guidelines and support inspections.
  • Responsible for BRR and coordination of batch release.
  • Manage Deviations and Complaints as QA representative.

Skills

GMP knowledge
Regulatory knowledge
German language
English language
Organization skills

Education

Bachelor's degree in science/technical field

Tools

SAP

Job description

Manager Quality Assurance Operations (m/f/d)

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!

Your Key Responsibilities:

Your responsibilities include, but not limited to:

  • Manage portfolio of projects, support a discipline and / or provide a service. If applicable, may provide functional expertise in area of responsibility.
  • Create and review GMP relevant documents in own area of responsibility (e.g. batch records for material manufactured and packaged internally, SOPs, procedures, records, third party work)
  • Negotiate and clarify deficiencies in GMP documents in area of own responsibility with the
  • Provide support to internal policies (GOPs, Manual), and global compliance initiatives.
  • Develop and improve GMP processes to meet internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority guidances, SOPs, HSE etc.).
  • Organize, coordinate Pest Control program tasks. Supervise external partners for pest control.
  • Prepare reports and risk assessments in area of responsibility.
  • Promote and enforce compliance to guidelines.
  • Support inspections and audits and perform self-inspections and audits if applicable.
  • Responsible for BRR and coordination of batch release.
  • Support artwork changes as respective quality role.
  • Responsible for Deviations and Complaints as QA representative.
  • Management of quality data in SAP
What you’ll bring to the role:
  • Basic degree in scientific, technical or relevant discipline
  • (BS or equivalent) or comparable education / experience
  • Basic scientific, technical and regulatory knowledge in a
  • specific area
  • Good knowledge of cGMPs and working knowledge
  • Basic organization skills
  • Good knowledge in German and English
Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Hiring decisions are only based on the qualification for the position, regardless of gender, ethnicity, religion, sexual orientation, age and disability.

The law provides for severely disabled / equal applicants the opportunity to involve the local representative body for disabled employees (SBV) in the application process. If you would like to request this, please let us know in advance as a note on your CV.

Compensation Structure & Criteria:

Sandoz compensation is determined by job level, qualifications, niche skills, experience, and location within company salary ranges. Fully proficient and highly effective employees can expect a starting salary around market median, with those new to the level or with less functional depth at the lower end of the range and those with sustained superior or niche skills towards the higher end of the range. Internal equity and external market data inform our range placement. Annual salary reviews consider performance outcomes, market alignment, and business needs.

  • Starting pay range: EUR 54,100 - 100,500
  • Variable compensation: 5% performance-based bonus
  • Additional benefits includes: 30 vacation days per year (in full time), 1.200€ vacation payment (in full time), €40/month in capital-forming benefits (in full time), company pension, flex-hybrid working 50% per week in the office, access to our learning & development platforms Skillsoft & Learnlight, Access to our employee share program “OurShare”
  • Pay frequency: Monthly
  • Expected weekly working hours: 40 hours
  • Contract type: full time
Why Sandoz?

Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic human right of good health.

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.

Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported!

Join us, help us make healthcare fairer and faster.

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