Manufacturing Associate III

Experis Switzerland

Bezirk Solothurn

Vor Ort

CHF 60.000 - 90.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Eine zielgenaue Bewerbung für diesen Job — ein maßgeschneiderter Lebenslauf und ein Anschreiben, die genau zur Stellenanzeige passen.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Experis Switzerland is seeking a Manufacturing Associate for a 5-shift rotation including nights in Luterbach, Solothurn. Start date 21.09.2026; end date 28.02.2027.

The role requires 3–5 years of experience in a cGMP environment, strong documentation, and the ability to work independently while collaborating with on-site teams. You will be responsible for daily manufacturing operations, equipment maintenance, and ensuring compliance with health, safety, and environmental regulations.

Qualifikationen

  • 3–5 years of experience in manufacturing.
  • Experience in a cGMP environment and operation of process equipment.
  • Strong documentation skills and training maintenance.
  • Ability to work independently with minimal direction.
  • Good verbal and written communication skills.
  • Commitment to safety and EH&S regulations.
  • Maintain training curriculum and follow procedures.

Aufgaben

  • Perform and document daily manufacturing operations in a cGMP environment.
  • Operate process equipment and execute validation protocols.
  • Maintain equipment and facilities and ensure regulatory compliance.
  • Maintain training levels and support other functions on site.
  • Collaborate with supporting functions to achieve best outcomes for patients and the facility.
  • Demonstrate accurate documentation and record-keeping for all activities.
  • Consult supervisor or manager when in doubt and communicate issues clearly.
  • Ensure adherence to safety principles and regulatory procedures.

Kenntnisse

Detail-oriented
Documentation
Independent worker
Verbal communication
Written communication
Collaborative
Biopharmaceutical knowledge

Jobbeschreibung

General Information:
Start Date: 21.09.2026
End Date: 28.02.2027
Location: Luterbach, Solothurn
Shift work: 5 Shift rotation (including nights)

  • Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents.
  • Ensuring compliance to cGMP as well as maintaining equipment and facilities.
  • The Manufacturing Associate is detail-oriented with strong documentation skills. Maintain training level to the required level and support other functions on site.
  • Assist with daily manufacturing operations in manufacturing facility. Typically requires 3-5 years of experience.
  • The employee will be responsible for executing manufacturing related work within Solothurn as per procedures and policies.
  • The employee will be accountable for maintaining and complying with the environmental, health and safety regulations.
  • The employee will be responsible for maintaining his/hers training curriculum and not perform tasks that the employee is not trained to perform.
  • Be able to work independently and with minimal direction. Has moderate responsibility.
  • The employee will be responsible for maintaining equipment and perform manufacturing activities. Erroneous work can impact product integrity result inbatch failures and consequently harm patients.
  • The employee must be able to demonstrate the ability to independently document and record information related to their job functions.
  • The employee must at all times make sure that if the employee is in doubt that the employee’s supervisor or manager is consulted. Good verbal and written skills are required to ensure proper description of any issues.
  • Employee must collaborate well with supporting functions and seek to define best outcomes forpatients and the facility.
  • A basic knowledge of biopharmaceutical technology and processes. The employee must be able to follow and comply with procedures and protocols.
  • The employee should occasionally be able to make routine decisions based on gained experience. The employee must have a solid understanding of the requirements within correct and timely documentation within a cGMP environment.
  • The employee must be trained and skilled in all operational and regulatory procedures of manufacturing department.
  • Employee understands importance of safety and can teach saftey principles to less experienced colleagues.
Hol dir deinen kostenlosen, vertraulichen Lebenslauf-Check.
oder ziehe deine Datei hierhin.
Similar jobs

Ähnliche Jobs, die dir auch gefallen könnten

Manufacturing Associate III
Manufacturing Associate III

Experis Schweiz • Bezirk Solothurn

Vor Ort
CHF 65.000 - 90.000
Manufacturing Associate III
Manufacturing Associate III

Swisslinx • Bezirk Solothurn

Vor Ort
CHF 90.000 - 110.000
Biopharma cGMP Manufacturing Associate III
Biopharma cGMP Manufacturing Associate III

Experis Schweiz • Bezirk Solothurn

Vor Ort
CHF 65.000 - 90.000
Senior Manufacturing Associate (Downstream and Upstream Processing)
Senior Manufacturing Associate (Downstream and Upstream Processing)

Randstad Switzerland • Luterbach

Vor Ort
CHF 100.000 - 130.000
cGMP Manufacturing Specialist III – Night Shift
cGMP Manufacturing Specialist III – Night Shift

Experis Switzerland • Bezirk Solothurn

Vor Ort
CHF 60.000 - 90.000
cGMP Manufacturing Specialist III
cGMP Manufacturing Specialist III

Swisslinx • Bezirk Solothurn

Vor Ort
CHF 90.000 - 110.000
Manufacturing Associate Level III (a)
Manufacturing Associate Level III (a)

Michael Page • Bezirk Solothurn

Vor Ort
CHF 70.000 - 110.000
Extension option
Manufacturing Associate III
Manufacturing Associate III

Swisslinx AG • Bezirk Solothurn

Vor Ort
CHF 90.000 - 120.000
Manufacturing Associate Level III (a)
Manufacturing Associate Level III (a)

Michael Page International (Switzerland) SA • Bezirk Solothurn

Vor Ort
CHF 70.000 - 90.000
Extension option
Process Engineer m/f/d
Process Engineer m/f/d

Aristo Group • Luzern

Vor Ort
CHF 90.000 - 130.000