Associate Specialist Manufacturing Process Excellence, Boudry
Associate Specialist Manufacturing Process Excellence, Boudry
-
Boudry, Schweiz
-
Aufgegeben: vor weniger als einem Monat
-
Merken
Anzeigentext
Position overview: Supports manufacturing process documentation, equipment commissioning and troubleshooting, and continuous improvement initiatives. Focuses on writing technical documentation, participating in equipment qualification activities, and ensuring timely closure of quality records.
Responsibilities
Provide expertise in manufacturing processes
Write technical documentation
Participate in commissioning, FAT/SAT, IOQ, PQ, and operational readiness as part of new equipment
Write system requirement definition and associated supporting quality records and documentation (e.g., change management) to support equipment enhancement post-product commercialization or manufacturing process
Support data integrity risk assessment
Prepare and assist operations teams with new equipment set-up and troubleshooting
Participate in equipment qualification tasks.
Deploy, maintain, and execute level 1 maintenance
Act as primary point of contact for equipment troubleshooting
Write lockout/tagout documentation (e.g., ECP)
Participate in A3 problem‑solving initiatives related to technical topics
Own and lead local continuous improvement initiatives.
Provide technical expertise for investigation, CAPAs, process improvement, and other various topics upon request
Ensure on‑time closure of quality records (e.g., CAPA, action, document periodic review)
Own and lead change control at the discretion of the production team
Additional duties and responsibilities may be assigned as needed to meet business requirements.
Qualifications
Bachelor's degree or equivalent in a technical discipline.
0–2 years of experience in pharmaceutical operations.
Understanding of GMP and technical processes.
Proficiency in French (mandatory) and English.
This job description is not intended to be exhaustive; additional duties and responsibilities may be assigned as needed to meet business requirements.
Equal Employment Opportunity Statement: BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles. Applicants may request accommodations prior to accepting an offer.
Location: Los Angeles County (if applicable). For additional information, please refer to the BMS California residency page.
Data protection: BMS will never request payments, financial information, or social security numbers during the application process. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Job Title: R1601990 Associate Specialist Manufacturing Process Excellence
#J-18808-Ljbffr
Responsibilities
Provide expertise in manufacturing processes
Write technical documentation
Participate in commissioning, FAT/SAT, IOQ, PQ, and operational readiness as part of new equipment
Write system requirement definition and associated supporting quality records and documentation (e.g., change management) to support equipment enhancement post-product commercialization or manufacturing process
Support data integrity risk assessment
Prepare and assist operations teams with new equipment set-up and troubleshooting
Participate in equipment qualification tasks.
Deploy, maintain, and execute level 1 maintenance
Act as primary point of contact for equipment troubleshooting
Write lockout/tagout documentation (e.g., ECP)
Participate in A3 problem‑solving initiatives related to technical topics
Own and lead local continuous improvement initiatives.
Provide technical expertise for investigation, CAPAs, process improvement, and other various topics upon request
Ensure on‑time closure of quality records (e.g., CAPA, action, document periodic review)
Own and lead change control at the discretion of the production team
Additional duties and responsibilities may be assigned as needed to meet business requirements.
Qualifications
Bachelor's degree or equivalent in a technical discipline.
0–2 years of experience in pharmaceutical operations.
Understanding of GMP and technical processes.
Proficiency in French (mandatory) and English.
This job description is not intended to be exhaustive; additional duties and responsibilities may be assigned as needed to meet business requirements.
Equal Employment Opportunity Statement: BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles. Applicants may request accommodations prior to accepting an offer.
Location: Los Angeles County (if applicable). For additional information, please refer to the BMS California residency page.
Data protection: BMS will never request payments, financial information, or social security numbers during the application process. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Job Title: R1601990 Associate Specialist Manufacturing Process Excellence
#J-18808-Ljbffr
Highlights
-
FirmennameBristol Myers Squibb
-
JobtitelAssociate Specialist Manufacturing Process Excellence
Sicherheitstipps
Lehnen Sie Jobangebote ab, die im Voraus Geld für Arbeitsmaterialien verlangen.
Weitere Informationen zur Anzeige
Die Anzeige Associate Specialist Manufacturing Process Excellence wurde bei Locanto in der Rubrik Neuenburg Ingenieurwesen veröffentlicht.
Wenn Sie noch mehr passende Angebote suchen, schauen Sie sich auch Ingénieur environnement ou génie civil spécialisé en … in Neuchâtel in dieser Rubrik an.
Es gibt noch weitere Kleinanzeigen im Umkreis von 15 km in dieser Rubrik. Klicken Sie hier, um sich die Anzeigen anzusehen.