Sr Manufacturing Technician

RemoteWorker US; Social Circle (GA); On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a dedicated production professional to ensure compliance with cGMP and safety regulations. This role involves hands-on execution of manufacturing operations, problem-solving across departments, and training team members. You will be pivotal in maintaining high standards of quality and efficiency in production processes. Join a company that values patient care and is committed to fostering an inclusive environment where your contributions can make a real difference. This is an exciting opportunity to grow in a dynamic setting while ensuring the delivery of quality products to patients in need.

Benefits

Medical insurance

Dental insurance

Vision insurance

401(k) plan with company match

Paid vacation

Paid sick time

Tuition reimbursement

Paid volunteer time off

Qualifications

• 4+ years of related work experience or 2+ years with an associate's degree.
• Knowledge of laboratory and pharmaceutical production equipment.

Responsibilities

• Assist supervisor in organizing and directing team members.
• Main interface with other departments to resolve equipment and process issues.

Skills

cGMP knowledge

problem-solving

quantitative analysis

communication skills

leadership skills

Education

High school diploma or GED

Associate's degree or higher

Tools

Microsoft Word

Microsoft Excel

laboratory equipment

Job description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

About the role:

The role is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. In addition to being fully accountable and involved in all production processes, he/she may problem solve in other functional areas. The incumbent acts as a delegate to the supervisor and may conduct departmental activities in their absence. He/She fully understands the regulations and may make recommendations according to their interpretations. He/She is responsible for the successful transfer of new processes/methodologies into the manufacturing area.

How you will contribute:

• Assist supervisor in organizing, scheduling and directing other team members.
• Main interface with other departments to resolve issues related to equipment, process, compliance, including maintenance, metrology, and validation.
• Involved in hands-on execution of manufacturing operations.
• Ensure timely and accurate generation of process documentation. Review documentation.
• Resolve issues related to equipment, process and compliance. Main troubleshooting/response person.
• Investigate any process problems timely and provide documentation.
• Participate on Continuous Improvement Teams and may serve in a leadership role.
• Train and mentor other team members and monitor training for newer team members.
• Assist with process/equipment validation and data analysis.
• Assign other project work and/or involvement in teams to team members.
• Represent the department in cross functional teams as necessary.
• May perform other duties as assigned.
• Knowledge of cGMP manufacturing and in-depth process knowledge of related manufacturing techniques/specialties.
• Thorough knowledge of laboratory and pharmaceutical production equipment including but not limited to autoclaves, process tanks, incubators, analytical equipment and CIP/SIP systems.
• Must be able to apply quantitative analysis to analyze process performance.
• Incumbent must be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurement.
• Must be able to read and follow detailed written instructions and have good verbal/written communication skills. Good procedural writing skills.
• Knowledge of chemical and biological safety procedures.
• Good computer skills, knowledge of Microsoft Word and Excel.
• Must have demonstrated interpersonal and leadership skills and be able to lead a work team effectively and efficiently in a team environment.

What you bring to Takeda:

• Requires a high school diploma or GED plus 4+ years of related work experience or associates’ degree or higher and 2+ years related work experience.

Important Considerations

At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:

• Must be able to carry up to 25 lbs., lift up to 50 lbs., and push/pull > 100 lbs. (with the assistance of material handling equipment).
• Must be able to stand for extended periods of time over an entire 8 or 12-hour shift.
• Must be able to climb ladders and stairs while wearing special gowning.
• May require bending, twisting, reaching overhead, and/or squatting motions to perform certain tasks.
• May be required to work in a confined area.
• Some Clean Room and cool/hot storage conditions.
• May require immunization before performing work within the manufacturing area.
• May work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.
• Will need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.
• May work in a cold, hot or wet environment.
• May work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.
• Must be able to work multiple shifts, including weekends. Must be able to work overtime as required.

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Locations

USA - GA - Social Circle - Hwy 278

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job Exempt

No