Associate Specialist Upstream Operations (m/f/d) Shape the Future of Biologics Bring Your GMP Expertise to the Next Level
Duration: ASAP – 1 year (temporary)
About Our Client For our client, an innovative and internationally oriented biotech company in the greater Lucerne area, we are looking for an experienced Associate Specialist Upstream Operations (m/f/d). The company specialises in the GMP-compliant manufacturing of biological drug substances for early-phase clinical trials, leveraging cutting-edge technologies and a strong commitment to continuous innovation in biopharmaceutical production.
Your Responsibilities
Hands-on execution and troubleshooting of upstream manufacturing processes in a GMP-regulated environment
Drafting, updating, and technical review of SOPs and electronic master batch records related to process transfers and GMP manufacturing
Active contribution to continuous improvement initiatives and support for the integration of new technologies, including non-GMP engineering runs
Material management via ERP systems (SAP) and coordination of supply-related tasks
Participation in sampling activities, including occasional on-call or weekend duties as required by process scheduling
Ensuring full compliance with GMP principles and EHS standards within the area of responsibility
Your Profile
Academic background in a relevant discipline (Bachelor's or Master's degree in biotechnology, life sciences, or a related field)
Minimum 1–2 years of practical experience in the pharmaceutical or biotech industry
Prior hands-on experience with biologics manufacturing under GMP, ideally including shake flask work, wave systems, and single-use bioreactors
Familiarity with automated manufacturing systems (e.g. DeltaV) and electronic batch record platforms (e.g. PAS‑X) is a strong advantage
Ability to work effectively under pressure in a complex GMP environment, with a proactive and solution-oriented mindset
Business fluent in German (C1) and English (B2+), both written and spoken
Residence within approximately 30 minutes of Schachen (LU), driver's licence (B) required
Ready to take the next step in your biotech career? We'd love to connect with you! Apply now as an Associate Specialist Upstream Operations (m/f/d) in Schachen (LU) and let's shape the future of biologics manufacturing together.
#J-18808-Ljbffr
Duration: ASAP – 1 year (temporary)
About Our Client For our client, an innovative and internationally oriented biotech company in the greater Lucerne area, we are looking for an experienced Associate Specialist Upstream Operations (m/f/d). The company specialises in the GMP-compliant manufacturing of biological drug substances for early-phase clinical trials, leveraging cutting-edge technologies and a strong commitment to continuous innovation in biopharmaceutical production.
Your Responsibilities
Hands-on execution and troubleshooting of upstream manufacturing processes in a GMP-regulated environment
Drafting, updating, and technical review of SOPs and electronic master batch records related to process transfers and GMP manufacturing
Active contribution to continuous improvement initiatives and support for the integration of new technologies, including non-GMP engineering runs
Material management via ERP systems (SAP) and coordination of supply-related tasks
Participation in sampling activities, including occasional on-call or weekend duties as required by process scheduling
Ensuring full compliance with GMP principles and EHS standards within the area of responsibility
Your Profile
Academic background in a relevant discipline (Bachelor's or Master's degree in biotechnology, life sciences, or a related field)
Minimum 1–2 years of practical experience in the pharmaceutical or biotech industry
Prior hands-on experience with biologics manufacturing under GMP, ideally including shake flask work, wave systems, and single-use bioreactors
Familiarity with automated manufacturing systems (e.g. DeltaV) and electronic batch record platforms (e.g. PAS‑X) is a strong advantage
Ability to work effectively under pressure in a complex GMP environment, with a proactive and solution-oriented mindset
Business fluent in German (C1) and English (B2+), both written and spoken
Residence within approximately 30 minutes of Schachen (LU), driver's licence (B) required
Ready to take the next step in your biotech career? We'd love to connect with you! Apply now as an Associate Specialist Upstream Operations (m/f/d) in Schachen (LU) and let's shape the future of biologics manufacturing together.
#J-18808-Ljbffr
Scientific Associate Arbeitgeber: nemensis ag Schweiz
Unser Kunde ist ein innovatives und international ausgerichtetes Biotech-Unternehmen in der Region Luzern, das sich durch eine dynamische Arbeitsumgebung und ein starkes Engagement für kontinuierliche Innovation auszeichnet. Die Mitarbeiter profitieren von einer offenen Unternehmenskultur, die Teamarbeit und persönliche Entwicklung fördert, sowie von attraktiven Weiterbildungsmöglichkeiten und einem flexiblen Arbeitszeitmodell. Hier haben Sie die Chance, Ihre GMP-Expertise in einem zukunftsorientierten Umfeld einzubringen und aktiv an der Gestaltung der biologischen Arzneimittelproduktion mitzuwirken.
