Biological Services II (2nd Shift)

Spectraforce Technologies; Swiftwater (Monroe County); On-site; USD 28,000 - 39,000; Full time

Job summary

Spectraforce Technologies, Inc. is hiring for Biological Services II (2nd Shift) in Swiftwater, PA to perform production activities in the Biological Service Area (BSA).

This onsite role runs from 2 PM to 10:30 PM for an 8+ month assignment and focuses on producing quality materials per cGMP standards. Responsibilities include sampling, SAP inventory movements, cycle counting, documentation, and collaboration with Senior/Lead Technicians and Managers to maintain efficient operations while

Qualifications

• Strong self-driven work ethic with communication and time management.
• Attention to detail and good documentation skills.
• Must have basic mechanical aptitude and computer skills.
• Thorough knowledge of cGMPs and regulatory requirements are required.

Responsibilities

• Performs production in accordance with volume fluctuation, business need, and procedures in the Biological Service Area (BSA).
• Manufacturing activities in the assigned area.
• Completes sampling and corresponding documentation.
• Completes process order and bin to bin movements to ensure accurate SAP inventory.
• Participates in inventory management (SAP, cycle counting, ordering).
• Completes tasks and documentation per cGMP.
• Works with Senior/Lead Technicians and Managers to ensure efficient operation.
• Participates in team meetings and communicates improvement ideas and issues.

Skills

Strong self-driven work ethic

Communication skills

Time management

Attention to details

Ability to lift 30+ lbs

cGMP knowledge

Documentation skills

Job description

Position Title

Biological Services II (2nd Shift)

Work Location

Swiftwater PA, 18370

Assignment Duration

8+ Months

Work Arrangement

Onsite

Shift Timings

2 PM to 10:30 PM

Position Summary

• Performs production in accordance with volume fluctuation, business need, and effective procedures in the Biological Service Area (BSA).
• This position is responsible for manufacturing activities in the assigned area.

Key Responsibilities

• Completes sampling and corresponding documentation as required.
• Completes process order and bin to bin movements in an accurate and timely manner to ensure accurate inventory in SAP.
• Participates in all aspects of inventory management (SAP, cycle counting, ordering, etc.).
• Completes tasks and corresponding documentation as required by cGMP.
• Works with Senior and Lead Technicians as well as Managers to ensure an efficient operation.
• Participates in team meetings. Actively communicates improvement ideas, issues, concerns, etc. to team members.
• Identifies all production issues and relays them to the leadership team.
• Complete tasks such as environmental monitoring and water sampling to be completed.
• Write and edit cGMP procedures and documents under supervision.
• Participates in both deviation investigations when appropriate and implementation plans to ensure a quality product in all areas.
• Ensures proper process area operation by pre and post run set up and maintenance of lab and equipment.
• Works to complete quality documentation (BPR's, logbooks, etc.) accurately in a timely manner.

Qualification & Experience

• Strong self-driven work ethic with communication and time management skills.
• Commitment to personal and professional development by completing training.
• Adaptability in a changing work environment required to work in an area where various items enter and exit to support facility demands across site.
• Attention to details
• Good documentation skills
• Ability to work independently and in a group
• Requires good mechanical skills
• Must have basic mechanical aptitude, computer skills, good comprehension skills, retention skills, troubleshooting and manual dexterity.
• Thorough knowledge of cGMPs and regulatory requirements are required.
• Efficient, 10-hours on feet per day
• Ability to lift 30+ lbs.
• Detail oriented and ability to write clearly
• Self-driven and motivated
• Follow cGMP SOP/ SWI's for compliance
• Ability to work multiple shifts inclusive of weekends
• Years of Experience: 3 - 6 Years