Manufacturing Associate - Shift 2

Spectraforce Technologies; Summit (NJ); On-site; USD 36,000 - 48,000; Full time

Job summary

Spectraforce Technologies seeks a Manufacturing Associate for a 6-month assignment in Summit, NJ. The role involves producing blood component lots in a cGMP clean room under supervision, following SOPs and GDPs, and collaborating with a cross-functional team.

Training starts with 9:00 AM - 5:00 PM for 1-2 weeks, then shifts to the MO Quad schedule. Requires biology/chemistry knowledge and basic math, with MS Office proficiency.

Qualifications

• Bachelor's degree or equivalent with 2 years manufacturing experience, or HS diploma with 4 years experience.
• GMP clean room experience preferred.
• Ability to work in a team and follow SOPs.

Responsibilities

• Produce blood component lots through cell culture, harvest, and cryopreservation.
• Maintain aseptic technique for welding, connections, and transfers.
• Weigh and measure in-process materials to ensure correct quantities.
• Adhere to production schedule and internal logistics.
• Record production data clearly per GDPs.
• Work in a cross-functional team to complete shift tasks.
• Lead a team within a function, supervised by the shift supervisor.
• No direct reports.
• Performs other duties as assigned.

Skills

Cell culture basics

cGMP/FDA knowledge

Math skills

Technical writing

MS Office

Biology/Chemistry background

Education

Bachelor's/Assc. or Medical Tech degree with 2 years exp

HS diploma/GED with 4 years exp

Job description

Position: Manufacturing Associate

Duration: 06 Months

Location: Summit West, NJ, 07901

Breyanzi activation MO QUAD SCHEDULE:

Breyanzi MO Associate Shift 2 Tuesday- Saturday (1pm-10pm)

Training schedule

• The training period may range from 1 to 6 weeks, depending on business needs
• The selected candidate is required to maintain full availability, with no planned leave during the entire training period.
• Training will commence with a Monday to Friday, 9:00 AM - 5:00 PM schedule for the initial 1-2 weeks (subject to change based on business needs).
• Subsequently, the schedule will transition to the assigned Quad shift.

Description

Manufactures human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable.

Required Competencies: Knowledge/ Skills, and Abilities

• - Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique
• - Knowledge of cGMP/FDA regulated industry
• - Basic mathematical skills - General understanding of cGMPs
• - Technical writing capability
• - Proficient in MS Office applications
• - Background to include an understanding of biology, chemistry, medical or clinical practices Pre-requisites: Entry- Level

Duties and Responsibilities

• Production of blood component lots through cell culture, harvest, and cryopreservation.
• Aseptic technique is required for tube most activities: welding, connections, and transfers, at minimum.
• Weighs and measures in-process materials to ensure proper quantities are added/removed.
• Adheres to the production schedule ensuring on-time, internal production logistics.
• Records production data and information in a clear, concise, format according to proper GDPs.
• Works in a team based, cross-functional environment to complete production tasks required by shift schedule.
• Motivated, team consciousness individuals are needed to fulfill job requirements.
• Leads a team within a designated function of manufacturing, however, supervision will be managed by the shift Supervisor.
• No direct reports will be assigned to this job role.
• Performs other tasks as assigned.

Education and Experience

Bachelor's degree or Associate/ Medical Technical degree and 2 years of Manufacturing or Operations experience or High School diploma/GED and 4 years of Manufacturing or Operations experience

Important Notes about working in the clean room

This position takes place in a GMP clean room environment, which includes being gowned for up to 6 hours. During the processing time in the clean room, no breaks may be taken

Working Conditions

• - Intermittent walking and sitting to perform job functions; however, ability to sit or stand for extended periods of time may be necessary. - Physical dexterity sufficient to use computers and documentation.
• - Sufficient vision and hearing capability to work in job environment.
• - Ability to lift up to 25 pounds.
• - Must have the ability to work around laboratories and controlled, enclosed, restricted areas.
• - Cleanroom garments and personal protective equipment will be required in designated areas which cover head, parts of the face, core body, and legs/feet.
• - Makeup, gum, nail polish, or other potential microbial sources are prohibited in restricted areas.
• - Flexibility to don clean room garments and personal protective equipment (PPE).
• - Clean room environment is an enclosed, restricted space, with assigned pressure and temperature conditions. Reagents, chemicals, and exposure to sanitization agents are expected.
• - Routine exposure to human blood components.
• - Designated areas may prohibit food, any outside materials such as cell phones, tablets, at a minimum.

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other jobrelated duties as requested by management.