CQV Engineer (CIP, Chemicals, Clean Systems)
View: 240
Update day: 24-04-2024
Category: High Technology Mechanical / Technical Electrical / Electronics IT - Software
Industry: Research Biotechnology Pharmaceuticals
Position: Entry level
Job type: Full-time
Job content
Title: CQV Engineer (CIP, Chemicals, Clean Systems)Location: Visp, Switzerland
Rate: Open
Openings: 1 Engineer
Contract/Perm: Contract (12-Months)
A Fantastic new role has just opened up at one of our leading Swiss based clients offering the successful candidate the opportunity to join a hard-working team working on exciting projects in the pharmaceutical sector.
Responsibilities
- Self-manage CQ development and execution activities with respect to the relevant systems.
- Function as a key member of the CQ Team, and provide guidance regarding CIP + Chemical + Cleaning Systems.
- Maintain control over the activities and schedule with respect to the relevant systems.
- Participate in sessions to define/agree work breakdown structure with respect to the relevant systems
- Assist in assessing project risk and evaluating the effectiveness of mitigation strategies applied.
- Coordination and communication with other resources for CIP + Chemical + Cleaning Systems-related matters.
- Adherence to ORCA project procedures/requirements with respect to Health/Safety/Environmental, Quality (including GDP/GMP), CQ (including MCP, MQP, DQ, IQ, OQ, Commissioning).
- Liaise closely with the relevant vendors/providers/contractors, project Automation representatives and Construction-phase representatives to ensure integration of activities and schedules with respect to the relevant systems.
- Actively participate in the development and delivery of deliverables with respect to the relevant systems.
- Report on key deliverable and dates and align with key milestones within the project’s critical path.
- Report and aid in the resolution of project issues, including maintaining the non-conformance records.
- Assist in assessing project risk and evaluating the effectiveness of mitigation strategies applied.
- Prioritize and execute tasks in a fast-paced environment.
- Minimum Bachelor’s degree in Life Sciences or Engineering
- Minimum of 6+ (Lead) / 4+ (Senior) / 2+ (Intermediate) years of experience in commissioning / qualification / validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech industry.
- Proven CIP + Chemical + Cleaning Systems, and CIP knowledge.
- Minimum 6+ (Lead) / 4+ (Senior) / 2+ (Intermediate) years of experience in commissioning / qualification / validation of CIP + Chemical + Cleaning Systems.
- Experience with DeltaV (Emerson).
- Fluent English language written and verbal communication skills.
- cGMP knowledge and knowledge of regulatory requirements.
- Able to work with minimum oversight fulfilling deliverables within target dates.
- Fluent German is a distinct preference
- Experience with Lonza Commissioning / Qualification Approach.
- Experience with COMOS/KNEAT platforms.
- Biopharmaceutical knowledge
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Deadline: 08-06-2024
Click to apply for free candidate
Report job
SIMILAR JOBS
-
⏰ 26-05-2024🌏 Buchs (SG), St. Gallen SG
-
⏰ 26-05-2024🌏 Spiez, Bern BE
-
⏰ 26-05-2024🌏 Genève, Genève GE
-
⏰ 26-05-2024🌏 Zürich, Zürich ZH
-
⏰ 26-05-2024🌏 Delémont, Jura JU
-
⏰ 26-05-2024🌏 St. Gallen, St. Gallen SG
-
⏰ 26-05-2024🌏 Reinach (BL), Basel-Landschaft BL
-
⏰ 26-05-2024🌏 Wetzikon (ZH), Zürich ZH
-
⏰ 26-05-2024🌏 Thun, Bern BE
-
⏰ 26-05-2024🌏 Buchs (SG), St. Gallen SG