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Documentation Specialist; Installation Phase

Job in 3000, Bern, Canton de Berne, Switzerland
Listing for: Amtera
Full Time position
Listed on 2026-03-05
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Validation Engineer, Pharmaceutical Manufacturing, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Documentation Specialist (Installation Phase)

Bern

Project Based Contract

About Amtera:

Amtera is a leading consultancy specializing in tailored, flexible managed workforce solutions that drive project success across IT, engineering, life sciences, and project management. Our mission is to support these industries by providing intelligent, results-driven workforce solutions to clients across diverse sectors. We help optimize vendor ecosystems, control costs, and deliver results with precision through our extensive network of seasoned professionals.

Position Overview:

We are seeking a meticulous and experienced Documentation Specialist to join our team for a client in the API (Active Pharmaceutical Ingredient) manufacturing industry. This role focuses on the installation phase of a new site, ensuring all documentation is accurate, complete, and compliant with industry standards. The ideal candidate will have a strong background in documentation management within the pharmaceutical or API manufacturing sector.

Key Responsibilities:
  • Develop, compile, and manage documentation related to the installation phase of the new API manufacturing site.
  • Ensure all documentation complies with industry standards, including GMP, FDA, and EMA regulations.
  • Collaborate with engineering, construction, and quality teams to gather and verify documentation requirements.
  • Maintain accurate records of equipment installation, commissioning, and qualification activities.
  • Prepare and review Standard Operating Procedures (SOPs), work instructions, and other technical documents.
  • Ensure timely and accurate documentation of changes and updates throughout the installation process.
  • Manage document control processes, ensuring all documents are properly categorized, stored, and easily retrievable.
  • Conduct regular audits of documentation to ensure compliance and identify areas for improvement.
  • Provide training and support to project teams on documentation standards and procedures.
  • Liaise with external contractors and vendors to ensure proper documentation of installation activities.
Key Requirements:
  • Bachelor’s degree in a relevant field such as Engineering, Life Sciences, or Information Management.
  • Proven experience in documentation management within the pharmaceutical or API manufacturing industry.
  • In-depth knowledge of GMP, FDA, EMA, and other relevant industry standards and regulations.
  • Strong understanding of the installation and commissioning processes in an API manufacturing environment.
  • Excellent attention to detail and organizational skills.
  • Strong communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
  • Proficiency in document management systems and software.
  • Ability to manage multiple tasks and priorities in a fast-paced environment.
  • Familiarity with project management principles and practices is a plus.
  • Willingness to be on-site as required during the installation phase.
Why Join Us?
  • Opportunity to contribute to a high-impact project within the API manufacturing industry.
  • Collaborate with a team of experts dedicated to advancing engineering, technology, and compliance.
  • Be part of a forward-thinking company that values your professional growth and development.
  • Enjoy a dynamic and supportive work environment.

Amtera is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Fostering Advancement in Technology and Engineering

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