Responsible for providing strategic and operational leadership for the Quality function to ensure compliance with company quality requirements for footwear, leather, and raw materials while driving continuous improvement in quality performance, manufacturing processes, and team capability.
Compensation
The targeted hiring range for this full-time position is $99,700 - $134,600 depending on qualifications; however, the expanded salary range provides opportunities for advancement.
Responsibilities
Lead, coach, develop, and empower a high-performing quality organization through effective goal setting, performance management, talent development, succession planning, and continuous feedback
Build a proactive coaching culture that drives accountability, engagement, technical competency, and continuous improvement throughout the Quality function
Provide leadership for ensuring compliance with company quality standards, regulatory requirements, and customer expectations
Participate in the development and execution of quality strategies that optimize current capabilities while preparing the organization for future business needs
Lead quality improvement projects ensuring disciplined execution, proactive risk identification, effective corrective actions, and measurable business results
Senior Manufacturing Engineer responsible for designing, developing, and validating manufacturing processes for medical device products in the Abbott Vascular Devices division.
Compensation
$78,000.00 – $156,000.00
Responsibilities
Design and develop manufacturing processes for life sciences products
Develop procedures for economical mass production in cooperation with pilot-plant and production departments
Conduct tests and measurements throughout production stages
Troubleshoot and solve production process problems
Lead equipment and manufacturing process qualification activities (IQ, OQ, PQ)
Contribute to global health through innovative process development and optimization, providing technical leadership in technology transfer, process validation, and manufacturing support across facilities.
Compensation
The salary range estimated for this position based in Massachusetts is $83,300.00–$125,000.00.
Responsibilities
Lead technology transfer for the upstream cGMP manufacturing viral vectors and other modalities
Collaborate with other sites or clients to ensure success of process transfer and scale up
Ensure effective information flow, risk assessment, timeline execution, issue resolution and documentation for cross-functional teams
Authoring detailed process definition and facility fit assessment exercises
MST process leads for Upstream processes, ensuring the materials, strategy and documentation are in place
Requirements
Advanced Degree
Bachelor's Degree
Nice to have: adherent mammalian cells (HEK)
Nice to have: late stage/commercial technology transfer
Nice to have: cell and gene therapy vector production
The Operations Quality team partners with manufacturing, engineering, and technical functions to ensure compliance, process capability, product quality, and continuous improvement across manufacturing operations.
Compensation
Salary ranges for U.S (excl. PR) locations (USD):$79,200.00 - $118,800.00
Responsibilities
Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
Requirements
Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A)
Principal subject matter expert and process owner for end-to-end manufacturing of liquids and lyophilized parenteral products at Manatí, responsible for technology transfer, validation, optimization, and daily support of manufacturing processes.
Compensation
Manati - PR - US: $106,520 - $129,080
Responsibilities
Lead technology transfer projects and new product introduction teams
Develop and execute technology transfer plans
Integrate site time and event schedules
Perform Design of Experiments and Process Risk Assessment
Act as communication liaison for transfer, validation, and optimization activities
Requirements
Bachelor’s degree in Pharmacy, Engineering, Chemistry, or Science
Master’s degree with 6-9 years experience
PhD with 4-6 years experience
Nice to have: Three years experience in parenteral manufacturing of protein therapeutics
Provide scientific and technical leadership within Manufacturing Science & Technology and help develop site technical capabilities to support reliable manufacturing.
Compensation
The salary for this position is expected to range between $98,700 and $183,300 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.
Responsibilities
Provide scientific and technical leadership within Manufacturing Science & Technology and help develop site technical capabilities
Ensure robust product and process stewardship and end-to-end technical oversight throughout the commercial lifecycle
Own the site Validation Master Plan, ensuring manufacturing, packaging, and cleaning processes remain validated
Lead technical transfers and enable robust commercial scale-up and launch of new products
Drive technical excellence during operational start-up of new manufacturing equipment and areas
Provide scientific and technical leadership while developing the capabilities needed to support reliable manufacturing for the new Isotopes site.
Compensation
The salary for this position is expected to range between $98,700 and $183,300 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.
Responsibilities
Provide scientific and technical leadership within Manufacturing Science & Technology and help develop site technical capabilities
Ensure robust product and process stewardship and end-to-end technical oversight throughout the commercial lifecycle
Own the site Validation Master Plan, ensuring manufacturing, packaging, and cleaning processes remain validated
Lead technical transfers and enable robust commercial scale-up and launch of new products
Drive technical excellence during operational start-up of new manufacturing equipment and areas
Lead the product strategy and growth for Cretex Medical’s precision injection molding business, driving market expansion, technology roadmap, and profitability.
Compensation
USD $139,500.00 - USD $216,300.00 /Yr.
Responsibilities
Own the multi-year Molding Solutions roadmap
Expand advanced polymer, micro-molding, and tooling capabilities
Partner with OEM engineering teams for DFM and mold flow evaluations
Build ROI-based business cases for presses, cleanrooms, and automation
Lead technical quoting and pricing for tooling and production programs
Requirements
Bachelor’s degree in Plastics Engineering, Polymer Science, Mechanical Engineering, Materials Science, Business, or a related field
Nice to have: MBA
Nice to have: master’s degree in Plastics/Polymer Engineering
Nice to have: RJG Scientific Molding certification
Product Director - Molding SolutionsNewCretex Medical Component and Device Technologies · Brooklyn Park, US