Manufacturing Technician

Actalent; Worcester (MA); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading company in engineering and sciences services seeks a Manufacturing Technician in Worcester, MA. In this entry-level role, you'll support operations by following safety procedures, maintaining equipment, and conducting tests while receiving extensive onboarding training. Ideal candidates possess a degree in science and are adaptable problem-solvers ready to work in a fast-paced environment.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Employee Assistance Program

Short and long-term disability

Qualifications

• 1 year manufacturing experience preferred.
• Knowledge of cGMP operations is preferable.
• Strong written and verbal skills.

Responsibilities

• Following precise procedures in cGMP environment while prioritizing safety.
• Conducting sampling and performing in-process analytical testing.
• Managing inventory levels and participating in shipping of finished materials.

Skills

Adaptability

Problem-solving

Communication

Judgment

Education

Bachelor's Degree in Science

Associate Degree/Equivalent Certification

Job description

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Description

Job Description: Manufacturing Technician As a Manufacturing Technician you'll collaborate with our talented engineers quality experts and cross-functional teams to execute crucial functions that drive our operations. You'll have the opportunity to leverage state-of-the-art programs such as LIMS SAP automated control systems DCS PLC PI and more. One of the unique advantages of joining this team is our comprehensive 6-week onboarding training program exclusively designed for our manufacturing technicians. You'll receive the support and resources needed to excel in your role right from the start. Responsibilities: As a key member of our team you'll take on a diverse range of responsibilities that encompass Upstream Downstream and Core Support functions. Your key responsibilities may include: - Following precise verbal and written procedures in a controlled cGMP environment while prioritizing safety regulations. - Meticulously documenting processes in corresponding batch records and log sheets adhering to cGMP and established Standard Operating Procedures. - Collaborating with our team to determine innovative process methods and procedures actively contributing to the continuous improvement of our operations. - Demonstrating a strong commitment to safety by diligently wearing personal protective equipment such as gowning safety glasses gloves and safety shoes. - Proactively completing and maintaining training requirements to stay up to date with the latest industry standards. - Occasionally going above and beyond by working overtime to meet project deadlines and deliver exceptional results. - Managing inventory levels and actively participating in the shipping of finished materials. - Conducting sampling and performing in-process analytical testing to guarantee product quality and integrity. - Skillfully preparing equipment for operation including cleaning and sterilization processes CIP/SIP. - Performing pH and conductivity measurements crucial parameters for process control and optimization. - Operating manufacturing equipment such as glass washers and autoclaves. - Contributing to the preparation of buffers and media vital components of our production activities. - Engaging in cell culture activities ranging from vial thaw to production scale. - Responsible for performing key column operations Tangential Flow Filtration TFF and load line setup. Qualifications: We are seeking talented individuals with various experience levels to join our Manufacturing Technician team. To qualify you should possess: - Bachelors Degree in a science discipline is highly preferred with 1 year manufacturing experience. - Associate degree/equivalent certification required with1 year manufacturing experience preferred. - Knowledge of cGMP operations is preferable. - The ability to exercise considerable judgment and initiative as you'll be working on assignments that require critical decision-making. - A deep understanding of the implications of your work and the capacity to make well-informed recommendations for effective solutions. - The capability to determine appropriate methods and procedures when faced with new assignments showcasing your adaptability and problem-solving skills. Physical Safety Requirements: To thrive in this role you should meet the following physical and safety requirements: - Strong written and verbal skills enabling effective communication. - The ability to read written instructions and/or numbers at close and far ranges. - Comfortable working with a computer or tablet for 50-60 of scheduled work time. - The ability to thrive in a manufacturing environment with a constant sound level of 75 decibels which is comparable to the sound of a washing machine. Occasional use of hearing protection may be required to ensure your well-being. - Adaptability to spending 50 of your scheduled work time in a stationary position where your focus and attention to detail will be paramount. - Frequently move and position yourself to observe equipment readings ensuring accurate monitoring and data collection. - Work with your team to transport/move equipment weighing up to 50 lbs. with support from appropriate safety equipment. Your safety is our top priority. - Key Job Posting Requirements: o Must posses professional demeanor o Come thoroughly prepared to interview o MUST be flexible working OT hours or OT additional days o Provide shift secondary shift preference o Provide screening questionnaire with resume submittal o Need email confirming offer details are agreed/accepted o Candidates submitted for this position must be eligible to work in the United States without company sponsorship now or in the future for employment based work authorization. Interview Process o 1 round interview 1 hour 30 minutes in person interview Application Screening questions ***Must be included on the candidate resume*** Name: 1. Please describe your familiarity with biologics processing at-scale equipment in solution preparation cell culture purification and/or equipment cleaning/preparation areas. Answer: 2. Please describe a skill you believe will be your biggest strength in this role. If this will be a change in career or discipline please describe a key skill you see as being transferrable to a biologics manufacturing role. Answer: 3. Please describe a leadership opportunity or challenge you have had to-date. Answer: 4. Can you please explain if youve worked in an environment that required personal protective equipment? If so have you ever recognized an unsafe situation at work and what did you do? Answer: 5. Please rank from highest 1 to lowest 10 the shift preference the candidate is interested in working or N/A for any shifts not available to work. Answer: Shift Days Hours Duration Preferred order 1 through 10 or N/A 1st shift Mon to Fri 6a to 2:30p 5 x 8hr 2nd shift Mon to Fri 2p to 10:30p 5 x 8hr 1st shift Sun to Wed 5a to 3:30p 4 x 10hr 1st shift Sun to Wed 6a to 4:30p 4 x 10hr 2nd shift Sun to Wed 2p to 1230a 4 x 10hr 2nd shift Sun to Wed 4p to 2:30a 4 x 10hr 1st shift Wed to Sat 4:30a to 2:30p 4 x 10hr 1st shift Wed to Sat 6a to 4:30p 4 x 10hr 2nd shift Wed to Sat 2p to 12:30a 4 x 10hr 2nd shift Wed to Sat 4p to 2:30a 4 x 10hr

Pay And Benefits

The pay range for this position is $28.00 - $30.80/hr.

Description

Job Description: Manufacturing Technician As a Manufacturing Technician you'll collaborate with our talented engineers quality experts and cross-functional teams to execute crucial functions that drive our operations. You'll have the opportunity to leverage state-of-the-art programs such as LIMS SAP automated control systems DCS PLC PI and more. One of the unique advantages of joining this team is our comprehensive 6-week onboarding training program exclusively designed for our manufacturing technicians. You'll receive the support and resources needed to excel in your role right from the start. Responsibilities: As a key member of our team you'll take on a diverse range of responsibilities that encompass Upstream Downstream and Core Support functions. Your key responsibilities may include: - Following precise verbal and written procedures in a controlled cGMP environment while prioritizing safety regulations. - Meticulously documenting processes in corresponding batch records and log sheets adhering to cGMP and established Standard Operating Procedures. - Collaborating with our team to determine innovative process methods and procedures actively contributing to the continuous improvement of our operations. - Demonstrating a strong commitment to safety by diligently wearing personal protective equipment such as gowning safety glasses gloves and safety shoes. - Proactively completing and maintaining training requirements to stay up to date with the latest industry standards. - Occasionally going above and beyond by working overtime to meet project deadlines and deliver exceptional results. - Managing inventory levels and actively participating in the shipping of finished materials. - Conducting sampling and performing in-process analytical testing to guarantee product quality and integrity. - Skillfully preparing equipment for operation including cleaning and sterilization processes CIP/SIP. - Performing pH and conductivity measurements crucial parameters for process control and optimization. - Operating manufacturing equipment such as glass washers and autoclaves. - Contributing to the preparation of buffers and media vital components of our production activities. - Engaging in cell culture activities ranging from vial thaw to production scale. - Responsible for performing key column operations Tangential Flow Filtration TFF and load line setup. Qualifications: We are seeking talented individuals with various experience levels to join our Manufacturing Technician team. To qualify you should possess: - Bachelors Degree in a science discipline is highly preferred with 1 year manufacturing experience. - Associate degree/equivalent certification required with1 year manufacturing experience preferred. - Knowledge of cGMP operations is preferable. - The ability to exercise considerable judgment and initiative as you'll be working on assignments that require critical decision-making. - A deep understanding of the implications of your work and the capacity to make well-informed recommendations for effective solutions. - The capability to determine appropriate methods and procedures when faced with new assignments showcasing your adaptability and problem-solving skills. Physical Safety Requirements: To thrive in this role you should meet the following physical and safety requirements: - Strong written and verbal skills enabling effective communication. - The ability to read written instructions and/or numbers at close and far ranges. - Comfortable working with a computer or tablet for 50-60 of scheduled work time. - The ability to thrive in a manufacturing environment with a constant sound level of 75 decibels which is comparable to the sound of a washing machine. Occasional use of hearing protection may be required to ensure your well-being. - Adaptability to spending 50 of your scheduled work time in a stationary position where your focus and attention to detail will be paramount. - Frequently move and position yourself to observe equipment readings ensuring accurate monitoring and data collection. - Work with your team to transport/move equipment weighing up to 50 lbs. with support from appropriate safety equipment. Your safety is our top priority. - Key Job Posting Requirements: o Must posses professional demeanor o Come thoroughly prepared to interview o MUST be flexible working OT hours or OT additional days o Provide shift secondary shift preference o Provide screening questionnaire with resume submittal o Need email confirming offer details are agreed/accepted o Candidates submitted for this position must be eligible to work in the United States without company sponsorship now or in the future for employment based work authorization. Interview Process o 1 round interview 1 hour 30 minutes in person interview Application Screening questions ***Must be included on the candidate resume*** Name: 1. Please describe your familiarity with biologics processing at-scale equipment in solution preparation cell culture purification and/or equipment cleaning/preparation areas. Answer: 2. Please describe a skill you believe will be your biggest strength in this role. If this will be a change in career or discipline please describe a key skill you see as being transferrable to a biologics manufacturing role. Answer: 3. Please describe a leadership opportunity or challenge you have had to-date. Answer: 4. Can you please explain if youve worked in an environment that required personal protective equipment? If so have you ever recognized an unsafe situation at work and what did you do? Answer: 5. Please rank from highest 1 to lowest 10 the shift preference the candidate is interested in working or N/A for any shifts not available to work. Answer: Shift Days Hours Duration Preferred order 1 through 10 or N/A 1st shift Mon to Fri 6a to 2:30p 5 x 8hr 2nd shift Mon to Fri 2p to 10:30p 5 x 8hr 1st shift Sun to Wed 5a to 3:30p 4 x 10hr 1st shift Sun to Wed 6a to 4:30p 4 x 10hr 2nd shift Sun to Wed 2p to 1230a 4 x 10hr 2nd shift Sun to Wed 4p to 2:30a 4 x 10hr 1st shift Wed to Sat 4:30a to 2:30p 4 x 10hr 1st shift Wed to Sat 6a to 4:30p 4 x 10hr 2nd shift Wed to Sat 2p to 12:30a 4 x 10hr 2nd shift Wed to Sat 4p to 2:30a 4 x 10hr

Pay And Benefits

The pay range for this position is $28.00 - $30.80/hr.

Eligibility requirements apply to some benefits and may depend on your job

classification and length of employment. Benefits are subject to change and may be

subject to specific elections, plan, or program terms. If eligible, the benefits

Available For This Temporary Role May Include The Following

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
  
  

Workplace Type

This is a fully onsite position in Worcester,MA.

Application Deadline

This position is anticipated to close on Jun 20, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [e-mail] for other accommodation options.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Management and Manufacturing

• Industries

  Business Consulting and Services

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