Manufacturing Associate IV

Manpower Switzerland is a leading provider of job placement services, helping over 20,000 men and women find permanent or temporary positions each year.

With a network of over 5,000 client companies, ranging from SME's to multinationals, Manpower connects talented individuals with opportunities in various industries.

The company is dedicated to providing high-quality services and is committed to supporting professional development and career growth.

The Manufacturing Associate IV performs and documents daily manufacturing operations in a cGMP environment. This includes operating process equipment, executing validation protocols, and revising cGMP documentation.

The role ensures compliance with cGMP standards while maintaining equipment and facilities. The ideal candidate possesses a strong understanding of automated systems and process controls, is detail-oriented, and maintains necessary training levels to support functions on site.

Principal Accountabilities

Executes manufacturing processing steps and / or manufacturing support activities : Monitors processes against the recipe and manufacturing documentation.

Example : Ensures proper operation of equipment during production runs.

Percent of Time Spent : 65%

Performs troubleshooting / investigation of equipment and process issues : Identifies and resolves equipment or process issues to minimize downtime.

Example : Investigates deviations in manufacturing processes and implements corrective actions.

Percent of Time Spent : 10%

Revises documents as instructed, Capable of equipment and / or process changes : Updates documentation according to instructions and participates in equipment or process changes.

Example : Modifies standard operating procedures based on process improvements.

Percent of Time Spent : 5%

Actively participates in training activities : Manages individual training plan and trains other associates as required.

Example : Provides training on new equipment or procedures to team members.

Percent of Time Spent : 5%

Executes validation protocols : Conducts validation activities to ensure compliance with regulatory requirements. Example : Performs equipment qualification tests as per validation protocols.

Percent of Time Spent : 5%

Capable of leading shift when supervisor is absent : Leads or participates in shift exchanges, coordinating activities with cross-functional areas.

Example : Assumes leadership responsibilities during supervisor's absence and ensures smooth operations on the manufacturing floor.

Percent of Time Spent : 5%

And other job duties that may be assigned from time to time.

Percent of Time Spent : 5%

Minimum Education Requirements

Minimum educational level : Relevant education from the chemical industry, food industry, pharmaceutical, or biotech industry.

D. Minimum Experience Requirements

• High school diploma or equivalent experience and typically 9-11 years of relevant experience in the Pharma / Biotech industry OR Bachelor's degree in a related field with 5-6 years of Pharma / Biotech professional experience OR Bachelor's degree in an unrelated field and typically 7-9 years of Pharma / Biotech experience
• Good understanding of Delta V, Syncade, or similar automated systems
• Understanding of the full Biotech process
• Languages : English B1, German, and / or French an asset

If you are interested in this position, we look forward to receiving your application.