Verpackungstechnik-Experte Pharma - GMP & Prozessoptimierung
Merz Aesthetics GmbH
Merz Aesthetics ist ein unabhängiges, international tätiges Unternehmen im Bereich der ästhetischen Medizin. Unser umfassendes Produktportfolio gehört seit Jahren zu den qualitativ hochwertigsten innerhalb ihrer Kategorie und wird von Health Care Professionals weltweit geschätzt. Wir von Merz Aesthetics sind Teil der Merz-Gruppe und haben unsere EMEA-Zentrale in Frankfurt am Main. Unser globales Headquarter befindet sich in Raleigh, North Carolina, USA. Tagtäglich setzen wir uns mit mehr als 2.500 Mitarbeiter*innen in 26 Ländern dafür ein, die Schönheit der Haut wiederherzustellen und zu erhalten. Möchtest Du Teil unserer Erfolgsgeschichte werden? Dann starte bei Merz Aesthetics! Am Standort im Biopharmapark ist unser eigenständiges Produktionswerk auf Erfolgskurs. Wir befinden uns in einer gesunden Wachstumsphase und bieten einen sicheren Arbeitsplatz, an dem du deine Erfahrung und Ideen mit großer Eigenverantwortung einbringen kannst. Warum bewerben wir uns bei Dir? Weil wir uns freuen, wenn du deine Erfahrung und Ideen im folgenden Bereich einbringen möchtest: Das sind deine Aufgaben Ansprechpartner und Betreuung der übertragenen Verpackungsanlagen und Prozesse Erstellung von relevanten SOPs/ Verpackungsdokumentation für die übertragenen Anlagen und Prozesse und Sicherstellung der Aktualität und Konformität dieser SOPs Meldung und Bearbeitung relevanter Abweichungen an den übertragenen Anlagen und Prozessen Initiierung, Bearbeitung und Umsetzung von Verpackungsänderungen zur Verbesserung der Verpackungsprozesse Mitarbeit bei Bewertung von Prozessen und Verfahren im Verpackungsbereich (RA, Berichte) Mitwirkung bei Qualifizierungen/Validierungen Unterstützung bei der erforderlichen Schulung des Verpackungspersonals Mitarbeit bei der Vorbereitung von Selbstinspektionen und Behördeninspektionen sowie Abarbeitung der resultierenden Maßnahmepläne Mitarbeit bei Lean- und OPEX-Themen im Verpackungsbereich zur Effizienzsteigerung Konzeptionelle Weiterentwicklung (Prüfung und Bewertung) der Verpackungstechnologie mit dem Ziel der Erhöhung Effektivität, Nachhaltigkeit und der Sicherung der Qualität in Zusammenarbeit mit dem Fertigungsleiter Schnittstelle zum Bereich Engineering/ Maintenance Damit überzeugst Du uns Bachelor- oder Masterabschluss im ingenieurtechnischen oder naturwissenschaftlichen Bereich (vorzugsweise Verpackungstechnik oder eine vergleichbaren Fachrichtung) Mind. 5 Jahre Berufserfahrung in der pharmazeutischen Industrie und in der Herstellung von Arzneimitteln und/oder Medizinprodukten Sehr gute GMP-Kenntnisse Sehr gutes technisches Verständnis/ Prozesskenntnisse Sehr gutes analytisches Denk- und Ausdruckvermögen sehr gute Englischkentnisse in Wort und Schrift Einschlägige Kenntnisse bei den Officeanwendungen Teamorientiertes Arbeiten, Zuverlässigkeit, Belastbarkeit sehr gute Kommunikationsfähigkeit Das bieten wir Dir Mensch im Mittelpunkt: Bei uns erwartet dich eine offene Arbeitskultur mit flachen Hierarchien und kurzen Entscheidungswegen. Du wirst mit Kolleg*innen aus der ganzen Welt zusammenarbeiten. Und solltest du in eine Lebenslage kommen, in der du Beratung oder Hilfe benötigst, unterstützt dich unser Employee Assistance Programm Familie & Beruf: Unsere Mitarbeiter*innen sollen ihr Familien- und Berufsleben bestmöglich in Einklang bringen können. Ausgewogene Work-Life-Balance: Unsere Lebenszeit ist kostbar, unser Alltagsrhythmus individuell. Damit du Arbeit und Freizeit in deinem Sinne vereinbaren kannst, setzen wir auf zeitgemäße flexible Arbeitszeitmodelle. Wir bieten dir Gleitzeit sowie mobiles Arbeiten. Unsere Mitarbeiter*innen profitieren außerdem von großzügigen Urlaubsregelungen. Weiterbildungen: Deine persönliche und fachliche Weiterentwicklung ist für uns der Schlüssel zum Erfolg. Dazu führen wir regelmäßige Entwicklungsgespräche und ermöglichen verschiedenste Führungs- und Fachtrainings, Soft Skill Trainings, eLearnings, Sprachkurse und Coachings. Vergütung: Dich erwartet eine leistungsgerechte Entlohnung, wir zahlen nach dem Manteltarifvertrag für die chemische Industrie (Ost) #J-18808-Ljbffr Merz Aesthetics GmbH
- ...organization in North Carolina is seeking a Packaging Technician to manage and operate machinery within the packaging area, adhering to strict GMP and FDA guidelines. Candidates must have a high school diploma and three years of experience in the packaging industry....Suggested
- United Therapeutics is looking for a pharmaceutical manufacturing professional in Durham, North Carolina. The role requires expertise in GMP environments and production processes. Candidates should possess at least a high school diploma and have substantial hands-on...Suggested
- ...requires extensive experience in pharmaceutical or biotech environments, coordination across cross-functional teams, and knowledge of GMP regulations. Responsibilities include managing workflow processes, supporting PSSR activities, and overseeing RFIs to ensure project...SuggestedContract work
- ...qualifications protocols. The ideal candidate possesses strong organizational skills, communication abilities, and 2-5 years of experience in a GMP facility. Comprehensive benefits including medical coverage, 401(k), and employee stock options are offered. #J-18808-Ljbffr Merck &...SuggestedFull time
$35 - $42 per hour
...manufacturing team in Rocky Mount, NC. The ideal candidate will have over 8 years of HVAC maintenance experience, including 2 years in a GMP environment. Responsibilities include identifying system deficiencies and coordinating HVAC maintenance. The position offers...SuggestedHourly pay- ...Upstream systems, ensuring timely review of crucial documentation and facilitating GMP processes. The ideal candidate will have extensive experience with Upstream Equipment on large-scale projects and must be a Subject Matter Expert in the field. #J-18808-Ljbffr QCS Staffing
- A leading pharmaceutical manufacturing partner is hiring a QC Analyst in Raleigh, NC. This role involves performing analytical and wet chemistry testing, conducting routine inspections, and maintaining compliance with FDA regulations. Candidates should have a bachelor’s...Shift work
- bekbg is seeking a Project Manager in Raleigh, North Carolina, to oversee construction projects, especially in pharmaceutical manufacturing. The successful candidate will manage budgets, schedules, and client relations while ensuring compliance with industry standards....
- A construction firm in Raleigh, North Carolina, is looking for a Project Manager to oversee projects valued up to $20M. The ideal candidate will have a BS/BA degree and at least five years of construction experience. Responsibilities include budget management, schedule ...For subcontractor
$120k - $145k
...Source is seeking a BIM Services Administrator for a pharmaceutical manufacturing client in Raleigh, NC. This role requires a Revit expert with extensive experience in model management and coordination across multi-discipline projects. Responsibilities include...$20 - $24 per hour
...manufacturing firm is seeking a Manufacturing Associate I in Research Triangle Park, North Carolina. The ideal candidate will support daily GMP production operations and manage material handling, as well as ensure compliance with documentation practices. Applicants should have...Hourly pay- ...Engineering, Chemistry, or Life Sciences and 3+ years of experience in the Pharmaceutical/Life Sciences industry, particularly in a GMP environment. Responsibilities include project planning, coordinating logistics, and ensuring client satisfaction throughout the process...
- ...This role involves performing microbiological tests, conducting environmental monitoring in cleanrooms, and ensuring compliance with GMP regulations. Candidates should have a Bachelor’s degree in a life science and at least 4 years of experience in a regulated lab environment...Contract work
- Catalent Pharma Solutions in Morrisville is seeking an Automation Engineer to support manufacturing efforts for inhaled products. You will... ...Group on new products and ensure automation designs adhere to GMP standards. The ideal candidate has a Bachelor’s degree in...
- Overview Build Advanced Pharma Systems. Travel Globally. Make an Impact. Brinox designs and delivers advanced process systems and GMP washers for the world’s leading pharmaceutical and biotech... ...equipment Learn, grow and become the expert on ‘your’ equipment Enjoy global...Work at officeRemote workFlexible hours
- ...folding sequences, pocket orientation, trim allowances, glue flaps, pharma N‑up limits). Select the appropriate press/printing process (... ...regulatory/quality requirements for pharma/medical packaging (GMP documentation, line clearance, traceability, insert/outsert...
$200k - $250k
...serve as a highly skilled subject matter expert, providing deep functional, technical, or... ...transfer activities from development into GMP manufacturing, including documentation, gap... ...experience in capital project engineering, pharma cGMP facility start‑up, CapEx/OpEx project...Full timeWork experience placementWork visa- ...and OneSource services. Job Title Validation Engineering (pharma) Consultant - Project Farma Location(s) Raleigh, NC... ...resolution or mitigation solutions. Ensure delivery of high-quality GMP Engineering services that meet client specifications, regulatory...Full timeFor contractorsWork experience placementLocal areaWork visa
- ...Position Responsibilities: Responsible for execution of all GMP instrumentation Maintenance and Calibration activities that are... .../ Core Competencies: Serves as a subject matter expert in metrology and metrology methodologies, providing technical guidance...Night shiftWeekend work
- ...pharmaceutical packaging. Responsibilities include following Master Batch Records, operating and cleaning equipment, and ensuring compliance with GMP standards. Candidates should have a high school diploma and preferred experience in pharmaceutical packaging. The position requires...Shift workDay shift
$284.32k - $355.4k
...Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc... ...international scientific meetings. · Serve as the subject matter expert for neurology, representing Clinical Research to both internal...WorldwideFlexible hours- ...practices, gowning, material handling, and data recording meet GMP standard ~ sPartner with Quality to ensure adherence to data integrity... ...and internal/external assessment sServe as a subject matter expert for production systems during regulatory interactions and...Contract work
$85k - $110k
A business consulting and services firm is seeking a highly motivated Process Engineer to join their team in Raleigh, NC. This entry-level position involves resolving technical issues, supporting equipment reliability, and ensuring compliance with regulatory standards. ...- ...involves operational readiness, SAP EWM implementation, and inventory processes. The ideal candidate will have some experience in a GMP environment and exposure to supply chain logistics. Strong communication and problem-solving skills are essential. This opportunity is...
$80k - $100k
A consulting firm in the pharmaceutical industry seeks a senior engineer with 8+ years in commissioning and qualification. The successful candidate will lead teams, engage in validation projects, and work closely with cross-functional departments in Raleigh, NC. Responsibilities...- Associate Supply Chain Engineer (Pharma | SAP EWM | Startup) We're looking for an Associate Supply Chain Engineer to support a pharmaceutical... ...with SAP EWM, inventory processes, and go‑live activities in a GMP environment. Summary Support warehouse readiness, go-live, and...
$145k - $200k
...focusing on Pharmaceutical specific projects. Previous Biotech/pharma experience is strongly preferred. This position can be performed... ...different contract types (e.g., Lump Sum, Guaranteed Maximum Price (GMP), Cost Plus). Lead document management for project, including...Contract workTemporary workWork at officeRemote workLong distanceFlexible hours- ...Industrial Engineer II CRB's over 1,100 expert professionals drive innovative, life-changing and life-saving solutions for manufacturers... ...and virtual commissioning strategies. Ensure compliance with GMP, FDA, and other regulatory standards in simulation-based design...
- ...exclusive features. Direct message the job poster from Planet Pharma The Business Development Manager effectively identifies and pursues... ...Consultant We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help...Full timeContract workFor contractorsWork at officeImmediate start
- Our client is a pharma company in Raleigh. The Packaging Supervisor is responsible for overseeing the packaging operations within a pharmaceutical... ...handling equipment. Knowledge of Good Manufacturing Practices (GMP) and safety regulations. Ability to work cross-functionally and...Weekend work
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