Cqv Engineer Drug Product Basel Biologics

Schweiz, Switzerland

Job Description

\\n CQV Engineer Drug Product \\xe2\\x80\\x93 Basel Biologics

Located in Basel area, Switzerland our successful Business Unit in Drug Product currently offers exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the position as Plant Engineer / CQV Engineer Drug Product Aseptic Manufacturing supporting a new sterile Drug product facility.

Key responsibilities:
  • Collaborate effectively during FATs, construction walkdowns, and C&Q activities to facilitate a seamless equipment hand-over process.
  • Following successful handover, take charge of ensuring the safe and cGMP-compliant operation of process equipment, along with the meticulous execution of maintenance activities.
  • Diligently manage tasks related to the upkeep of comprehensive and current system documentation.
  • Play a pivotal role in conducting risk assessments and crafting essential SOPs and work instructions for the new facility and equipment within your realm of responsibility.
  • Maintain the qualification status, prioritizing safety and cGMP compliance, across the designated areas.
  • Consistently and meticulously record and oversee data encompassing functional locations, equipment, spare parts, spare part lists, instruction manuals, SOPs, and more.
  • Keep meticulous records and maintain the historical data in SAP while ensuring that plant PIDs accurately reflect the current status.
  • Exhibit proficiency in handling deviations and changes across your entire sphere of responsibility. Serve as the subject matter expert (SME) for your area during inspections and audits.
Key requirements:
  • Hold an academic degree in engineering or a related field, or possess a comparable qualification in economics with a technical emphasis (e.g., HF, FH, Dipl. Ing. / M. Sc. / B. Sc.).
  • Exhibit a solid technical grasp and a profound understanding of engineering principles.
  • Offer extensive professional experience in Engineering and Operations within the Pharmaceutical Industry.
  • Proficiency in SAP-PM and MS Office is a fundamental requirement, with a proven track record of adeptly utilizing these tools.
  • Familiarity with GMP compliance requirements is a valuable asset, although not obligatory.
  • Demonstrate robust analytical skills, including the ability to define and measure key performance indicators (KPIs) and pinpoint areas for enhancement.
  • Possess fluency in both German and English, enabling seamless communication in a cross-cultural context.
Key Benefits:
  • Median salary of 110.000 CHF (based on years of experience, academic background and certifications)
  • Sign on bonus of 2.000 CHF on first payslip
  • Yearly bonus of 13%
  • Flat tax rate of 7-10%
  • Pension contribution of 60:40, employer-employee ratio (standard in Switzerland is 50:50)
  • Flight tickets, visa sponsorship for employee and family members
  • Salary per month per child (scalable based on age, starting from 380 CHF per month)
  • Opening of a bank account
  • Relocation of goods and furniture from abroad to designated address chosen by employee
  • 2 months of temporary accommodation
  • Support in search of permanent accommodation
  • 75% of travel reimbursement to and from work (commute)
  • 25 days of leave entitlement
  • Discounts for premium insurance
  • Additional employee only benefits (can be discussed over a call)
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Job Detail

  • Job Id
    JD1625571
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Schweiz, Switzerland
  • Education
    Not mentioned