The Junior Scientist – Level III applies advanced technical expertise in packaging processes and technologies within a regulated pharmaceutical environment. This role supports the implementation of new packaging technologies, leads process qualifications and validations, and ensures alignment with business goals, regulatory requirements, and company standards.
The incumbent is expected to lead cross-functional projects with limited supervision, troubleshoot complex packaging issues, and drive continuous improvement initiatives to enhance quality, efficiency, and compliance.
Key Responsibilities
Apply advanced technical solutions to packaging processes and technologies.
Lead packaging process qualifications, validations, and technology implementations.
Support the introduction of new products and changes to existing packaging processes.
Identify and implement process improvements related to quality, yield, efficiency, and compliance.
Provide technical support to packaging operations for quality investigations and issue resolution.
Analyze and resolve moderate to complex packaging process problems, developing both short- and long-term solutions.
Drive initiatives to improve packaging line efficiency and performance.
Develop and execute validation strategies for new packaging processes and configurations.
Support packaging technology transfer activities and ensure timely completion of action items.
Participate actively in regulatory inspections and support audit readiness activities.
Ensure all projects meet business, quality, and compliance objectives in alignment with cGMP and internal standards.
Collaborate with cross-functional teams including Quality, Manufacturing, Engineering, and Regulatory Affairs.
Qualifications
Education:
Bachelor’s Degree in Engineering (Industrial, Mechanical, Electrical, or related field)
Experience:
12–15 years of experience in the pharmaceutical or regulated industry
Prior supervisory or team leadership experience preferred
Technical Skills & Competencies
Strong knowledge of packaging processes in regulated environments
Experience with process validation and qualification (IQ/OQ/PQ)
Familiarity with cGMP requirements and regulatory expectations
Experience in technology transfer and new product introduction (NPI)
Strong troubleshooting and root cause analysis skills
Ability to lead cross-functional projects
Effective communication and collaboration skills
Strong analytical and problem-solving capabilities
Work Environment & Physical Demands
Combination of office and manufacturing floor environment
Ability to stand, walk, and move between areas as required
May involve moderate lifting
Ability to travel as needed
Equal Employment Opportunity (EEO) Statement
The Company is an Equal Opportunity Employer and is committed to providing a workplace free of discrimination and harassment. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other category protected by applicable federal, Puerto Rico, or local laws.
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