Sr Manufacturing Technician

BioSpace; Social Circle (GA); On-site; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Sr Manufacturing Technician to apply technical expertise in a dynamic environment. The role involves troubleshooting, mentoring, and executing manufacturing operations while ensuring compliance with cGMP standards. Candidates should possess a high school diploma or GED with relevant experience, along with strong communication and leadership skills. This position offers competitive compensation and benefits, including health insurance and paid time off.

Benefits

Health insurance

401(k)

Paid time off

Qualifications

• High school diploma or GED plus 4+ years of related experience.
• Knowledge of cGMP manufacturing and related techniques.
• Demonstrated leadership and interpersonal skills.

Responsibilities

• Assist supervisor in organizing, scheduling, and directing team members.
• Troubleshoot and resolve issues related to equipment, process, and compliance.
• Train and mentor team members, monitor training progress.

Skills

cGMP manufacturing

Quantitative analysis

Communication

Leadership

Interpersonal skills

Education

High school diploma or GED

Associate’s degree or higher

Tools

Microsoft Word

Microsoft Excel

Job description

Join to apply for the Sr Manufacturing Technician role at BioSpace.

Job Description

About the role:
As the Sr Manufacturing Technician, you will apply your technical expertise, gained from a high school diploma and relevant experience, to solve complex problems. You will work independently, serve as a resource for less experienced colleagues, and collaborate within and outside your department with minimal guidance.

How You Will Contribute

• Assist supervisor in organizing, scheduling, and directing team members.
• Interface with other departments to resolve issues related to equipment, process, and compliance.
• Execute manufacturing operations hands-on.
• Generate and review process documentation accurately and timely.
• Troubleshoot and resolve issues related to equipment, process, and compliance.
• Investigate process problems and document findings.
• Participate in Continuous Improvement Teams, possibly in a leadership role.
• Train and mentor team members, monitor training progress.
• Assist with process/equipment validation and data analysis.
• Assign project work and team involvement.
• Represent the department in cross-functional teams.
• Perform other duties as assigned.

Qualifications

• High school diploma or GED plus 4+ years of related experience, or an associate’s degree or higher with 2+ years of experience.
• Knowledge of cGMP manufacturing and related techniques.
• Familiarity with laboratory and pharmaceutical equipment.
• Ability to apply quantitative analysis and work with metric and US measurement systems.
• Strong reading, following instructions, and communication skills.
• Knowledge of chemical and biological safety procedures.
• Proficiency in Microsoft Word and Excel.
• Demonstrated leadership and interpersonal skills.

Physical and Environmental Requirements

• Ability to lift up to 50 lbs., carry up to 25 lbs., and push/pull over 100 lbs.
• Stand for extended periods, climb ladders, and work in controlled environments with gowning requirements.
• Work multiple shifts, including weekends, and overtime as needed.
• Work in cold, wet, or confined environments, and possibly require immunizations.

Compensation and Benefits

Hourly wage range: $20.53 - $32.26, dependent on experience and qualifications. Benefits include health insurance, 401(k), incentives, paid time off, and more.

Equal Opportunity Employment

Takeda is committed to creating a diverse workforce and providing equal employment opportunities.