Job title: BSA Lead Production Technician

Location: Swiftwater, PA

***THIS IS A 2nd SHIFT BSA LEAD PRODUCTION TECHNICIAN POSITION FOR BUILDING 59***

About the job

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster. 

 

About Sanofi 

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. 

Main Responsibilities:

• Performs production in accordance with business needs, and effective procedures. 

• Ensures all materials required for production are available prior to need. 

• Ensures the completion of sampling and corresponding documentation as required.

• Ensures the completion of move tickets and picklists in an accurate and timely manner to ensure accurate inventory. 

• Must have access to systems (SAP, Trackwise, and Labware).

• Must have access to systems in applicable buildings and processes which have these systems (SFD, PI, Metasys, Labwatch)

• Works to resolve all production issues. 

• Understands next steps and works to guide others through the process to complete them. 

• Understands science behind process steps and technology.

• Ensures all areas within the facility are adequately covered at all times. 

• Seeks out next steps and advises team as to what can be completed. 

• Ensures that the team is planning and working ahead whenever possible. 

• Completes tasks and corresponding documentation as required by cGMP Continues development by completing at least one developmental class annually. 

• Completes at least one developmental class outside of the core competencies annually.  

• Works to become trained in all assigned training modules.

• Training coordinator / Trainer –Train and guide Personnel in proper work procedures, use of equipment, cGMP’s, safe work techniques and SAP to assure timely signoffs and consistency in training.

• Maintains qualified trainer status. Follows all procedures put into effect to ensure your safety as well as the safety of others.

• Participates in monthly safety meetings. Utilizes +QDCI boards for Safety issues

• Reports all safety issues, concerns, incidents and near misses to the team leadership. 

• Actively participates in safety walkthroughs coordinated by the department’s safety team. 

• Provides input for potential safety issues as well as contributing ideas for corrective and preventative actions.

• Leads the safety team to ensure that the team is completing regular walkthroughs and is taking the necessary steps to address issues. 

• Works with both the safety and leadership team to ensure that the resources required to address safety issues are secured in a timely manner and that the effective resolutions are put into place and trained upon. 

• Works with the safety and leadership team to implement all safety initiatives by actively and effectively communicating the initiatives and by helping others to understand the initiatives.

• Ensures training is completed on all safety implementations.

• Follows effective procedures to ensure the production of a safe and efficacious product. 

• Has a thorough working knowledge of the cGMP’s and works to help others understand. 

• Identifies areas of deficiency and offers suggestions for improvements. 

• Identifies deviations and aids in investigations and root cause analysis. 

• Works to complete quality documentation (deviation investigations, BPR’s, logbooks, etc.) accurately in a timely manner. 

• Reviews quality documentation for completeness and releases commodities as required. 

• Understands the function of the quality group and works with them to maintain a positive rapport. 

• Works with the quality group/technical services group, as required, to ensure timely completion of deviation investigations, change controls, documentation, and CAPAs. 

• Ensures implementation of effective solutions to both deviations and deficiencies identified by our group or the quality unit.

• Participates/Leads in team meetings. 

• Actively communicates improvement ideas, issues, concerns, etc. to team members. 

• Participates/Leads in cross functional teams where necessary to complete projects in an effective and timely manner. 

• Works to help maintain positive working relationships between all team members. 

• Leads by example and works to help others understands the value in diversity. 

• Ensures that there are open lines of communication between all team members.  

• Assist in leading the shift change meetings and is responsible for assisting in the distribution of the shift change report. 

• Assist in ensuring that shift change reports and meetings are completed in an accurate, effective and timely manner.

• Mentors team members as it relates to the overall manufacturing process, situational awareness and previous lessons learned.

• Lead Operator or Room Lead or Subject Matter Expert within the BSA areas, that ensures quality and right the first-time efforts. 

• May provide leadership across one or more processing areas. May be responsible for scheduling of staff assignments, identifies issues and takes action to ensure that continuous incremental improvements are made in decreasing operator errors. 

• Informs managers of any production problems or concerns and recommends solutions. 

• Ensures processes / operations are documented in a timely and accurate manner. 

• Understands entire BSA process and demonstrates follow through in moving a process forward. Is aware of other departments and business areas, what they do, and how they fit into the overall objective of marketing and delivering products and services. 

• Systematically breaks down problems using standard approaches that have proven successful in the past.  

• Fully investigates and understands root causes of deviations in a step-by-step way. 

• Writes, reviews, and revises BPR’s, SOP’s and SWI’s as needed. 

• Continually monitors production activities with emphasis on safety, quality, efficiency and cost. 

• Cooperates willingly with colleagues, establishes rapport in a friendly and courteous manner. 

• Ensures site safety and HR policies are complied with and communicates issues immediately. Works with management to identify development opportunities for technician staff. 

• Coordinates the repair, PM’S and calibration of all equipment.

• All other duties as assigned 

 

About You

Requirements:

• Experience in a cGMP area.

• Prior or related experience recommended. 

• Must have knowledge and access to systems (SAP, key user access to SAP).

• Must have knowledge and access to systems in applicable buildings and processes which have these systems (SFD, PI). Must be qualified to complete BPR section reviews

• Requires good mechanical skills, computer skills and is detail oriented. Must have basic mechanical aptitude, good comprehension skills, retention skills, troubleshooting and manual dexterity.

Basic Qualifications:

• HS equivalent and 5+ in cGMP or Pharmaceutical experience

• Associates with 3+ in cGMP or Pharmaceutical experience

• Bachelor's with 2+ in cGMP or Pharmaceutical experience

Preferred Qualifications:

• Meet all Sr. Production Technician requirements.  

• Additionally have 1 + year leading teams in a Production environment and 1 + years training others in cGMP tasks

 

Why Choose Us?  

• Bring the miracles of science to life alongside a supportive, future-focused team. 

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. 

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. 

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave. 

Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. 

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Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

North America Applicants Only

The salary range for this position is:

$27.08 - $36.11

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.