Shift Manufacturing Engineer

• Contribute to Life Science projects for Antaes Asia clients
• Oversee the execution of manufacturing batches according to defined instructions, ensuring strict compliance with SOPs, training, and real-time monitoring of critical process steps for seamless operations.
• Collaborate on the development, review, and optimization of batch and cleaning recipes within DCS systems such as DeltaV and POMS, including manual and ad-hoc documentation.
• Lead or contribute to digitalization and continuous improvement initiatives aimed at enhancing process efficiency, reducing complexity, and supporting strategic site goals.
• Support troubleshooting efforts during process deviations or equipment issues by coordinating timely corrective actions with cross-functional teams.
• Provide training and guidance to chemical operators on operational best practices, equipment changes, OSW, and risk assessments.
• Participate in the commissioning, qualification, and validation phases of capital projects to ensure smooth integration into routine operations.
• Maintain compliance with environmental, health, and safety policies by participating in safety risk assessments and process hazard analysis as the operations representative.
• Ensure documentation accuracy by proactively resolving batch record discrepancies, contributing to investigations, and supporting timely CAPA implementation.
• Monitor shift deliverables, anticipate operational challenges, and ensure production timelines are met, highlighting potential delays to supervisors when necessary.
• Uphold plant readiness standards at all times, ensuring the facility remains audit-ready and operationally sound
• Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Description:

• Contribute to Life Science projects for Antaes Asia clients
• Oversee the execution of manufacturing batches according to defined instructions, ensuring strict compliance with SOPs, training, and real-time monitoring of critical process steps for seamless operations.
• Collaborate on the development, review, and optimization of batch and cleaning recipes within DCS systems such as DeltaV and POMS, including manual and ad-hoc documentation.
• Lead or contribute to digitalization and continuous improvement initiatives aimed at enhancing process efficiency, reducing complexity, and supporting strategic site goals.
• Support troubleshooting efforts during process deviations or equipment issues by coordinating timely corrective actions with cross-functional teams.
• Provide training and guidance to chemical operators on operational best practices, equipment changes, OSW, and risk assessments.
• Participate in the commissioning, qualification, and validation phases of capital projects to ensure smooth integration into routine operations.
• Maintain compliance with environmental, health, and safety policies by participating in safety risk assessments and process hazard analysis as the operations representative.
• Ensure documentation accuracy by proactively resolving batch record discrepancies, contributing to investigations, and supporting timely CAPA implementation.
• Monitor shift deliverables, anticipate operational challenges, and ensure production timelines are met, highlighting potential delays to supervisors when necessary.
• Uphold plant readiness standards at all times, ensuring the facility remains audit-ready and operationally sound
• Contribute to the promotion of Antaes services on top of assistance provided to clients

This is some text inside of a div block.

Job Requirements:

• Degree in Life Science, Chemical Engineering, Science or equivalent
• At least 2 years of experience in working in a GMP manufacturing environment is preferred
• Able to work comfortably in 12-hour rotating shift (Day/Night)
• Strong process knowledge and interest to guide and mentor
• High adaptability and ability to lead and work with cross functional team
• Strong communication and writing skills
• Excellent communication skills, both written and verbal

CDI

To join our Life Sciences team in Vaud, we are looking for aCompliance Specialist – Quality Control.

The project :

• Help the Quality Control (QC) team with daily compliance-related tasks.
• Investigate and manage issues like deviations and non-conformities.
• Review lab data to ensure it meets quality standards.
• Handle documentation for deviations, investigations, CAPAs, and change controls.
• Improve data integrity processes and report progress.
• Write, review, and update procedures and quality documents.
• Stay informed on new regulatory updates that affect QC.
• Prepare for audits and communicate with auditors and regulatory agencies.
• Suggest and implement process improvements.
• Support training and make sure the team follows compliance training.
• Work closely with QA and other departments to solve compliance issues.
• Provide training on GxP regulations and best practices.
• Stay current with industry standards and regulations.

CDI

CDI

• British Indian Ocean Territory +246
• British Virgin Islands +1
• Burkina Faso +226
• Cameroon (Cameroun) +237
• Canada +1
• Caribbean Netherlands +599
• Chad (Tchad) +235
• Chile +56
• Christmas Island +61
• Colombia +57
• Cook Islands +682
• Costa Rica +506
• Cuba +53
• Djibouti +253
• Dominica +1
• Eritrea +291
• Estonia (Eesti) +372
• Ethiopia +251
• Falkland Islands (Islas Malvinas) +500
• Finland (Suomi) +358
• France +33
• Gabon +241
• Grenada +1
• Guadeloupe +590
• Guam +1
• Guatemala +502
• Guernsey +44
• Honduras +504
• Iceland (Ísland) +354
• Ireland +353
• Isle of Man +44
• Italy (Italia) +39
• Jamaica +1
• Jersey +44
• Kiribati +686
• Malaysia +60
• Mali +223
• Marshall Islands +692
• Mauritius (Moris) +230
• Mayotte +262
• Montserrat +1
• Nauru +674
• Netherlands (Nederland) +31
• Niue +683
• Norfolk Island +672
• Northern Mariana Islands +1
• Norway (Norge) +47
• Paraguay +595
• Philippines +63
• Poland (Polska) +48
• Portugal +351
• Saint Helena +290
• Saint Kitts and Nevis +1
• Saint Lucia +1
• Saint Vincent and the Grenadines +1
• Samoa +685
• San Marino +378
• Solomon Islands +677
• South Africa +27
• Svalbard and Jan Mayen +47
• Togo +228
• Tonga +676
• Turkmenistan +993
• Turks and Caicos Islands +1
• U.S. Virgin Islands +1
• Uganda +256
• United Kingdom +44
• United States +1
• Uruguay +598
• Vanuatu +678
• Wallis and Futuna (Wallis-et-Futuna) +681
• Åland Islands +358

Drop a file here

Politique de confidentialité* En soumettant ce formulaire, vous reconnaissez avoir pris connaissance de la politique de confidentialité de notre site web qui inclut vos droits concernant vos données personnelles. J’accepte

Thank you Your submission has been received

Oops Something went wrong while submitting the form.

Shift Manufacturing Engineer

CDI

This is some text inside of a div block.

Job Description:

• Contribute to Life Science projects for Antaes Asia clients
• Oversee the execution of manufacturing batches according to defined instructions, ensuring strict compliance with SOPs, training, and real-time monitoring of critical process steps for seamless operations.
• Collaborate on the development, review, and optimization of batch and cleaning recipes within DCS systems such as DeltaV and POMS, including manual and ad-hoc documentation.
• Lead or contribute to digitalization and continuous improvement initiatives aimed at enhancing process efficiency, reducing complexity, and supporting strategic site goals.
• Support troubleshooting efforts during process deviations or equipment issues by coordinating timely corrective actions with cross-functional teams.
• Provide training and guidance to chemical operators on operational best practices, equipment changes, OSW, and risk assessments.
• Participate in the commissioning, qualification, and validation phases of capital projects to ensure smooth integration into routine operations.
• Maintain compliance with environmental, health, and safety policies by participating in safety risk assessments and process hazard analysis as the operations representative.
• Ensure documentation accuracy by proactively resolving batch record discrepancies, contributing to investigations, and supporting timely CAPA implementation.
• Monitor shift deliverables, anticipate operational challenges, and ensure production timelines are met, highlighting potential delays to supervisors when necessary.
• Uphold plant readiness standards at all times, ensuring the facility remains audit-ready and operationally sound
• Contribute to the promotion of Antaes services on top of assistance provided to clients

This is some text inside of a div block.

Job Requirements:

• Degree in Life Science, Chemical Engineering, Science or equivalent
• At least 2 years of experience in working in a GMP manufacturing environment is preferred
• Able to work comfortably in 12-hour rotating shift (Day/Night)
• Strong process knowledge and interest to guide and mentor
• High adaptability and ability to lead and work with cross functional team
• Strong communication and writing skills
• Excellent communication skills, both written and verbal

Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis. #J-18808-Ljbffr

---