Supervisor, Manufacturing Job at MSA BOURGOGNE (Otzolotepec)

Supervisor, Manufacturing

Location

Mexico , Toluca

Salary:

Not provided

MSA BOURGOGNE

Expiration Date

Until further notice

Requirements

2-4 years of experience

Job Responsibility

Impacts the level of service and the team’s ability to meet quality, volume, and timelines objectives within their area
Works within departmental objectives and priorities
Implements, interprets and executes policies
recommends modifications
Uses judgment to identify and resolve day-to-day problems
Decision making involves compiling and organizing information and selecting best option from well-defined alternatives

Supervisor, Manufacturing

BioMarin’s Technical Operations group is responsible for creating our drugs for ...

Location

United States , Novato

Salary:

83900.00 - 115390.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

B.S. degree in Life Sciences, Engineering, Applied Physics, etc., or acceptable equivalent combination of education and experience
4+ years of directly related industry experience, including at least 2+ years with proven leadership role
Ability to independently manage work, actions and expectations is essential
Strong knowledge and experience in all aspects of relevant process theory, equipment, and compliance
Proven experience with relevant process, theory and equipment
Experience with process automation and functionality
Complete understanding and adherence to cGMP’s as related to commercial operations
Current understanding of FDA and EMEA guidelines, cGMP's for Manufactured Drug Products
Experience with business systems (Process historian, LIMS, Trackwise, ERP, MES)

Job Responsibility

Accountable for the daily operations in area, requiring effective communication to make appropriate decisions, trouble shooting, and schedule adherences with minimal oversight
Accomplishes tasks through direct and effective coordination
Provides direction and hands-on training for staff
Management of staff
Fosters an environment of compliance, strong work ethic and ongoing learning
Ability to take responsibility for complex projects
Effective interaction with peers across manufacturing to create alignment and improvement
Partners with support groups (Facilities, Validation, Quality) to complete scheduled activities
Ability to troubleshoot, identify issues and support resolutions with technical groups
Required to perform ongoing operational tasks in respective work area

What we offer

company-sponsored medical, dental, vision, and life insurance plans
discretionary annual bonus
discretionary stock-based long-term incentives
paid time off

Fulltime

Supervisor, Manufacturing

The Manufacturing Supervisor leads a manufacturing team in a variety of complex ...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Minimum High School Diploma
5-7 years of experience in a GMPs environment required
3-5 years of experience leading direct reports or teams is preferred
Experience with GMPs, FDA and other regulated agency environments is required
Experienced in making real time decisions on safety, process, scheduling and personnel-related issues.
Ability to prioritize and manage multiple resources in a production environment with flexibility to meet organizational needs
Proven leadership, persuasiveness, initiative, and problem solving skills

Job Responsibility

Ensure safety of manufacturing area and work practices in accordance with all PCI Health, Safety and Environmental program.
Be highly visible, hands-on team builder to motivate, coach, support, inspire and retain highly effective teams while managing for high performance and developing others
Coordinate and supervise Manufacturing personnel in the cGMP operations to meet all scheduled manufacturing work
Partner with Planning to ensure effective prioritization and schedule adherence and to meet all required capacity demands
Guide and train employees to ensure FDA and other regulatory agency requirements have been properly implemented and are continually met.
Plan and execute manufacturing instructions in order to perform equipment preparation, and fill activities for aseptic and non-aseptic products in accordance with Good Manufacturing Practices (GMP)
Collaborate with the other supervisors and enabling groups to optimize processes
Recruit and supervise staff to execute department functions
ensure effective utilization of resources through consistent performance management
Provide leadership, guidance, and direction to staff in alignment with cGMP requirements, department goals and corporate quality standards

Fulltime

Supervisor, Manufacturing

Lead the manufacturing function within budget and output targets to meet custome...

Location

Malaysia , Batu Kawan, Penang

Salary:

Not provided

Sandisk

Expiration Date

Until further notice

Requirements

Minimum bachelor degree in management / engineering
Good knowledge in 6S / Safety & ESD production environment
Able to give full support during off/rest day as well (if required)
Able to work 12hours & Class 1K cleanroom

Job Responsibility

Lead the manufacturing function within budget and output targets to meet customer requirements and standards
Full accountability for ensuring safety, customer quality, cost and delivery requirements are met
Responsible for developing an enthusiastic, motivated and flexible team by building working relationships ensuring that Health, Safety and Environmental requirements are adhered to
Manage the team on best practice and establish standard policies and procedures whilst also mentoring and leading teams
Implement and manage continuous improvement and modern manufacturing principals by highlighting deficiencies and recommending changes in training, working practices and processes
Effectively and efficiently manage the production to meet the daily/weekly/monthly targets, meeting quality and delivery expectations, minimizing costs where possible and ensure the required best working practices are maintained at all times
Manage, coach and develop a high performing manufacturing team that meets agreed objectives, and which delivers best practice results, added value and continuous improvements
Ensure that the function operates in accordance with any health, safety and environmental policies and procedures to ensure the safety and wellbeing of workers and visitors
Maintains a high standard of 6S environment

Fulltime

New

Manufacturing Supervisor

Location

United States , Mountain Home

Salary:

80000.00 - 100000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

BS degree required with 0-3 years of manufacturing experience and 0-2 years supervisory experience
Demonstrated interpersonal and leadership skills with ability to interface well with other departments, and lead effectively and efficiently in a team environment
Demonstrated technical expertise in a manufacturing/technical environment
Ability to manage multiple priorities in a manufacturing plant setting
Strong professional writing skills and ability to prepare technical reports
Ability to understand GMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry
Strong assessment and troubleshooting skills
Good computer skills
Interact with all levels of personnel to analyze and solve problems related to manufacturing, Quality, documentation, and personnel issues
Work in and facilitate a team-oriented environment

Job Responsibility

Supervise the daily manufacturing operations in multiple areas – maintain (audit, refine, improve) equipment and processes within these areas across multiple shifts
Develop technical expertise to support team in daily execution, problem solving, and goal realization
Provide daily reports and communication on performance to goal, issue resolution, staffing, and personnel activities
Identify and implement continuous improvement initiatives in Safety, Quality, and Operations
Provide a positive and equitable working environment emphasizing the Baxter Shared Values – Respect, Responsiveness and Results
Support and Emphasize the Safety and Quality commitments of the department – make decisions concerning these commitments within the area
Ability to use resources and raw materials in the most efficient and productive manner possible
Identify/prioritize/provide resources in an area to assist the leadership team to meet the annual operational plan and budgetary commitments
Facilitate and verify appropriate training for employees in the area (including but not limited to GMP, job skills, safety)
Ensure compliance with all GMP rules, product documentation, specifications, SOPs, and FDA requirements as required

What we offer

medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
educational assistance programs
time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

New

Incoming Quality Control Supervisor, Manufacturing

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutio...

Location

United States , Austin

Salary:

Not provided

Diasorin

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Life Science or Engineering discipline
5 years of relevant experience in a hardware manufacturing environment in an FDA regulated industry and/or ISO certified organization with a Bachelor's Degree
8 years of relevant experience required with an Associate Degree
2 years of relevant Manufacturing Operations leadership experience

Job Responsibility

Provides direct supervision to the incoming inspection personnel and assures the effective use of all the resources to meet goals and requirements set forth by the Company and by Regulatory entities
Ensures Safety, Quality, GMP, ISO, and housekeeping standards are adhered to
Provides technical support and process improvement to minimize cost and increase productivity
Plays a key role in Lean Manufacturing Implementation
Supervises difficult inspection processes problems through a well and sound solution methodology
Ensures proper incoming inspection of components, packaging materials and final product in compliance with company procedures and ISO/FDA/GMP standards
Reviews inspection, labeling, and release logistic for appropriate process flow and documentation
Updates drawing, inspection procedures and any other documentation needed to inspect, test or purchase products
Oversees supplier quality metrics including but not limited to first pass yield
Collect and analyze data to track improvement and develop appropriate corrective actions, Conduct analysis, inspection, and trending in accordance with inspection plans work instructions and other quality standards to assure the quality of product or components

What we offer

competitive salary and benefits package

Fulltime

New

Manufacturing Supervisor

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

United States , Mountain Home

Salary:

80000.00 - 100000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

BS degree required with 0-3 years of manufacturing experience and 0-2 years supervisory experience
Demonstrated interpersonal and leadership skills with ability to interface well with other departments, and lead effectively and efficiently in a team environment
Demonstrated technical expertise in a manufacturing/technical environment
Ability to manage multiple priorities in a manufacturing plant setting
Strong professional writing skills and ability to prepare technical reports
Ability to understand GMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry
Strong assessment and troubleshooting skills
Good computer skills
Interact with all levels of personnel to analyze and solve problems related to manufacturing, Quality, documentation, and personnel issues
Work in and facilitate a team-oriented environment

Job Responsibility

Supervise the daily manufacturing operations in multiple areas – maintain (audit, refine, improve) equipment and processes within these areas across multiple shifts
Develop technical expertise to support team in daily execution, problem solving, and goal realization
Provide daily reports and communication on performance to goal, issue resolution, staffing, and personnel activities
Identify and implement continuous improvement initiatives in Safety, Quality, and Operations
Provide a positive and equitable working environment emphasizing the Baxter Shared Values – Respect, Responsiveness and Results
Support and Emphasize the Safety and Quality commitments of the department – make decisions concerning these commitments within the area
Ability to use resources and raw materials in the most efficient and productive manner possible
Identify/prioritize/provide resources in an area to assist the leadership team to meet the annual operational plan and budgetary commitments
Facilitate and verify appropriate training for employees in the area (including but not limited to GMP, job skills, safety)
Ensure compliance with all GMP rules, product documentation, specifications, SOPs, and FDA requirements as required

What we offer

medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
educational assistance programs
time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

New

Manufacturing Supervisor II

This is where we make life-saving products. You have deep knowledge of and exper...

Location

United States , Round Lake

Salary:

80000.00 - 110000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelors degree in Business, Engineering, related field or equivalent, is required
3 years manufacturing experience and 2 years of Supervisory experience
A candidate must not be allergic to Penicillin and Cephalosporin or their related products and minerals
Demonstrated communication, administrative and strong technical leadership skills with ability to interface well with other departments and lead effectively and efficiently in a team environment
Solid professional writing skills
Ability to lead multiple priorities in a manufacturing plant setting
Good assessment and troubleshooting skills (mechanical, electrical, and process) with demonstrated and confirmed experience and background
Proven understanding of maintenance systems to include preventive maintenance and CMMS
Ability to understand regulatory and safety guidelines applicable to the medical / pharmaceutical industry and industry in general
Must have experience and knowledge with Lockout / Tagout and other Safety Programs

Job Responsibility

Communicates guidance, support, direction and leadership through effective interactions with all personnel during daily operations
Supervises the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities
Identify/prioritize/provide resources as appropriate
Interviews, hires, coaches, motivates, develops, recognizes and leads performance of direct reports
Provides regular feedback to all direct reports
Assist in setting performance objectives and development plans and supervise progress
Reviews, approves, and handles documentation for batch and system records
Assists in release of product for distribution
Assists in meeting product release time goals
Identifies, initiates and facilitates continuous improvements, lean manufacturing activities and initiatives, such as 5S, visual management, kaizens

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement

Fulltime

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