Sorry, this listing is no longer accepting applications. Don’t worry, we have more awesome opportunities and internships for you.

cGMP Manufacturing Manager - Biotech

MEDVACON

cGMP Manufacturing Manager - Biotech

San Diego, CA
Full Time
Paid
  • Responsibilities

    Job Description

    MEDVACON is working with our BIOTECH CLIENT LOCATED IN SAN DIEGO ON A KEY POSITION FOR A CGMP MANUFACTURING/PRODUCTION MANAGER with a solid Biotech background. Our client is looking for a true blend of technical ability coupled with leadership and team building skills…someone ready for the next step in their career.  Lead and develop a growing functional area manufacturing, specifically involving small bulk molecule and oligonucleotide production.

    Responsibilities

    • Effectively and positively lead, train and advance team members to align with company goals and growth targets
    • A comprehensive review of process workflows to identify and implement continuous improvement opportunities
    • Analyze and manage work order releases with respect to capacity planning and material requirements
    • Lead development of a high performing manufacturing culture focused on critical KPI’s such as On-Time Delivery (OTD), Schedule Adherence, and Quality/First Time and Safe Lab Practices
    • Manages daily schedule with a focus on efficiency, meeting timelines, and maintaining a high quality of work
    • Manages maintenance, turnover, and availability of inventory to meet production demands
    • Ensures that manufacturing equipment is calibrated and maintained per SOP

    Qualifications

    • Bachelor’s degree in life sciences, or a related field
    • 2+ years of supervisory or management experience
    • 3+ years of experience with oligo synthesis, small molecule synthesis, nucleic acid purification processes[AW3] [AW4]
    • KNOWLEDGE OF MRNA, PLASMID OR CHEMISTRY IS REQUIRED

    The company has been operating for more than 20 years and still seeing tremendous growth….Base, bonus & full benefit package including medical, dental, vision, LTD, and a retirement plan.    Countless employee recognition and incentive programs and events.  Truly a great place to work...

  • Qualifications

    Qualifications

    Qualifications

    • Bachelor’s degree in life sciences, or a related field
    • 2+ years of supervisory or management experience in a Biotech setting
    • 3+ years of experience with oligo synthesis, small molecule synthesis, nucleic acid purification processes[AW3] [AW4]
    • KNOWLEDGE OF MRNA, PLASMID OR CHEMISTRY IS REQUIRED

    Additional Information

    NO! AGENCIES OR 3RD PARTY AGENCIES.  WE DO NOT WORK THROUGH OTHER EMPLOYERS

    THIS IS A POSITION directly with the client

    Please attach a WORD resume to your submission

    This is A FULL TIME POSITION W EXCELLENT BENEFITS 

    The work is ON-SITE All of your information will be kept confidential according to EEO guidelines. EOE/Veteran/Disabled