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Production Team Supervisor
vor 3 Monaten
Position Overview:
FERRING GmbH, a key player in the pharmaceutical manufacturing sector, is part of the globally operating and rapidly growing FERRING Group, headquartered in Switzerland. Our facility specializes in the production of critical pharmaceutical products in areas such as reproductive medicine, endocrinology, urology, pediatrics, and gastroenterology. We utilize state-of-the-art production technologies, focusing primarily on sterile dosage forms, particularly in the field of peptide hormones.
Your Role at Ferring:
We are currently seeking a Production Team Supervisor (m/f/d) for our production department. The successful candidate will also assume the role of Production Manager (m/f/d). This is a permanent full-time position.
Your Contribution to Meaningful Impact:
- Lead and manage a team of specialists with a focus on quality processes.
- Collaborate as a member of an integrated leadership team under the Associate Director of Production.
- Ensure compliance with legal regulations, Good Manufacturing Practices (GMP), manufacturing instructions, standard operating procedures (SOPs), and relevant pharmaceutical laws.
- Responsible for the creation, maintenance, and review of production-related instructions and conducting GMP-compliant training.
- Implement quality measures to ensure GMP-compliant production.
- Provide technical support for timely and GMP-compliant product manufacturing while maintaining consistent product quality.
- Assist in ensuring efficient and smooth production processes.
- Coordinate and manage deviation processes with the team.
- Accountable for quality metrics.
- Develop and coordinate sustainable corrective and preventive actions (CAPA) to enhance product quality.
- Create and review GMP-relevant documents in production.
- Co-manage the implementation of suitable pharmaceutical equipment, systems, and processes, including qualification and validation.
- Organize continuous improvement initiatives focused on quality enhancement.
- Act as a liaison for both internal departments (e.g., Engineering & Maintenance and Quality Assurance) and external parties (e.g., inspectors and auditors) regarding production matters.
- Contribute to the execution of local and global projects, particularly in harmonizing cross-departmental topics.
- Co-manage the advancement of continuous improvement measures and operational excellence initiatives.
Your Qualifications:
- A completed degree in natural sciences, engineering, business administration, computer science, or a related field.
- Several years of professional experience in the pharmaceutical industry, ideally in aseptic production or other highly regulated environments.
- A strong awareness of GMP, quality standards, and responsibilities, with practical experience in Annex 1.
- Hands-on experience with quality assurance systems and processes (Change Control, CAPA, deviations).
- A strong and motivating personality, preferably with initial leadership experience.
- High self-motivation and a willingness to take on responsibility.
- Problem-solving orientation and adeptness in handling conflict situations.
- Team-oriented with strong communication skills, along with a structured and goal-oriented work approach.
- Persuasive and assertive in both local and global contexts.
- Proficient in both German and English.
- Excellent knowledge of MS Office.
- Experience in applying Lean/Six Sigma methodologies and a strong willingness to actively initiate and support change processes.
- Willingness to work various shifts, including weekends.
