Pharmaceutical Assistant
Pfizer
2 hours ago
On-site
Kansas, United States
Operations
What You Will Achieve
- Organize and complete project tasks and milestones within deadlines.
- Develop and implement basic team effectiveness skills with your immediate team.
- Make basic problem-solving decisions under supervisory guidance with limited options.
- Adhere to established procedures in a structured work environment, consulting with colleagues as needed.
- Engage in collaborative communication with peers, supervisors, and interdepartmental teams to maintain a seamless drug production process.
- Oversee and address manufacturing processes, perform quality checks, and document procedures.
- Conduct cleaning and sanitization tasks as per procedures, ensuring files and databases are current.
- Assist in developing and implementing corrective actions in response to regulatory inspection feedback.
- Monitor processes for troubleshooting production issues regularly.
- Ensure all activities comply with company protocols and maintain high standards of quality control.
Here Is What You Need (Minimum Requirements)
- High school diploma (or equivalent) with at least 2 years of relevant experience
- Knowledge of cGMP and regulatory compliance
- Proficiency in using manufacturing equipment and tools
- Competence in troubleshooting and performing quality checks
- Demonstrated ability to follow established procedures and guidelines
- Experience with preparing and cleaning various components, materials, and equipment
- Strong organizational and documentation skills
Bonus Points If You Have (Preferred Requirements)
- Experience in pharmaceutical production
- Practical knowledge in a regulated industry
- Capability to work collaboratively within a team
- Ability to develop innovative ideas to simplify processes
- Commitment to professional development
- Strong communication skills
- Familiarity and basic understanding of common AI tools
Physical/Mental Requirements
- Correctable 20/20 vision; lift up to 40 lbs; sit and perform manual inspection for significant periods.
Non-standard Work Schedule
- 3rd shift M–T (1945–0615)
Other Job Details / Application Instructions
- Work location: On Premise
- Last day to apply: April 29th
- Organize and complete project tasks and milestones within deadlines.
- Develop and implement basic team effectiveness skills with your immediate team.
- Make basic problem-solving decisions under supervisory guidance with limited options.
- Adhere to established procedures in a structured work environment, consulting with colleagues as needed.
- Engage in collaborative communication with peers, supervisors, and interdepartmental teams to maintain a seamless drug production process.
- Oversee and address manufacturing processes, perform quality checks, and document procedures.
- Conduct cleaning and sanitization tasks as per procedures, ensuring files and databases are current.
- Assist in developing and implementing corrective actions in response to regulatory inspection feedback.
- Monitor processes for troubleshooting production issues regularly.
- Ensure all activities comply with company protocols and maintain high standards of quality control.
Here Is What You Need (Minimum Requirements)
- High school diploma (or equivalent) with at least 2 years of relevant experience
- Knowledge of cGMP and regulatory compliance
- Proficiency in using manufacturing equipment and tools
- Competence in troubleshooting and performing quality checks
- Demonstrated ability to follow established procedures and guidelines
- Experience with preparing and cleaning various components, materials, and equipment
- Strong organizational and documentation skills
Bonus Points If You Have (Preferred Requirements)
- Experience in pharmaceutical production
- Practical knowledge in a regulated industry
- Capability to work collaboratively within a team
- Ability to develop innovative ideas to simplify processes
- Commitment to professional development
- Strong communication skills
- Familiarity and basic understanding of common AI tools
Physical/Mental Requirements
- Correctable 20/20 vision; lift up to 40 lbs; sit and perform manual inspection for significant periods.
Non-standard Work Schedule
- 3rd shift M–T (1945–0615)
Other Job Details / Application Instructions
- Work location: On Premise
- Last day to apply: April 29th