Manufacturing Specialist III Job at Curia in Boston
Curia, Boston, Massachusetts, United States
Overview
MANUFACTURING SPECIALIST III in Hopkinton, MA
Build your future at Curia, where our work has the power to save lives
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.
The Manufacturing Specialist III will ensure timely manufacturing of all liquid and lyophilized parenteral cGMP products using aseptic processing technology to deliver high quality sterile products to the pharmaceutical industry. This role also provides shift support to manager and supervisor. The incumbent will manage daily manufacturing activities including scheduling, documentation, shift transfer meetings and performance reporting, and assist with duties in absence of shift manager/supervisor.
Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture
Benefits
Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!
Essential job duties
Must be available to work any shift, including day/nights/weekends
Own deviations, CAPAs, change controls, DCRs, equipment status
Perform GMP operations for upstream, downstream and RNA
Support buffer and media solution generation
Support all ancillary tasks associated with processing activities (assemblies, pH/conductivity meters, area cleanings, etc.)
Support process science with development batches
Help facilitate adequate completion of calibration, PM and new equipment implementation
Facilitate Root Cause Analysis for deviations and safety events, as needed
Create and revise SOPs and documents, SOP’s batch records and solution records
Participate in project meetings to ensure appropriate Manufacturing oversight and engagement
Drive activities to improve GMP best practices and suite cleanliness
Support continuous improvement projects
Education, experience, certification and licensures
Bachelor\’s degree in Science or related field or equivalent work experience
Minimum of 6-10 years’ directly applicable experience in the industry, including prior supervisory experience or equivalent combination of education and experience
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
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