<![CDATA[The Staffing Resource Group, Inc: jobboards]]>

<![CDATA[The Staffing Resource Group, Inc: jobboards]]> https://JOBS.SRG-US.COM/ en-us <![CDATA[Manufacturing Operator]]> Manufacturing Operator

Location: Miami, Florida
Industry: Pharmaceutical
Hours: 5pm-5am with rotating schedule. Week one is Friday, Saturday, Sunday and week two is Thursday, Friday, Saturday and Sunday. OT and weekends required. Training schedule is M-F, 5am-1:30pm or 1pm-9:30am or 9pm-5:30am up to 3 months.
Salary: $19.50/hr. plus 15% shift differential ($22.43/hr.)
Employment Type: Contract with the opportunity to go permanently based on performance and business needs. Multpile openings!

Environment: Our client is a dynamic specialty pharmaceutical company engaged in the research, development, manufacture, marketing, and sale of prescription pharmaceutical products. They are a leading developer of advanced transdermal drug delivery technologies and prescription transdermal products.

Position Overview: The Blending and Coating Manufacturing Operator performs all the general duties and operations to manufacture the product. An operator will operate machines and handle components using prescribed standard operating procedures and cGMP guidelines to manufacture and ensure the product meets the quality requirements. The operator will complete the necessary documentation and records to maintain quality control.

Responsibilities/Qualifications::

Operate punching, pouching and cartooning machines.
Operate blending, coating, and slitting machines.
Blend various ingredients for the coating process.
Perform set-ups and operate the equipment in the prescribed area of responsibility.
Assure work center operates safely to produce products within established quality standards within the cGMP and SOP guidelines.
Check and weigh components to ensure compliance.
Clean production room and equipment.
Perform duties as trained and assigned.
Maintain a clean organized work area.
Ability to follow oral and written instructions.
Ability to work in a fast-paced manufacturing environment.
Must meet medical requirements for personal protective equipment (PPE) used in manufacturing.
Ability to work with Controlled Substances and all required procedures.
Completes assigned training curriculums within assigned time frames before performing any activity associated with the training topic.
Ensure documentation is completed and meet the prescribed standards.

Education / Experience:

High school diploma. Candidate must demonstrate mechanical aptitude, ability to speak, read and write in the English language and demonstrate the ability to perform basic mathematical calculations.
Knowledge and experience with Outlook and basic computer proficiency in how to navigate computers.

Judgment / Decision Making:

Ability to ascertain that work complies with approved standards and meets the prescribed guidelines. Must be able to operate production equipment with minimal supervision from the LMO. Employee must demonstrate the ability of adhering to stringent documentation requirements.

Work Environment:

Plant floor, pharmaceutical products.

Physical Demands:

The employee is occasionally required to climb, balance, stoop, kneel, and crouch. Must demonstrate the ability to lift and or move 50 pounds or greater.

SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model partnering closely with clients to understand not only the role, but the company s culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.

ADA/EOE
IND123

]]> Tue, 13 Oct 2026 00:00:00 EDT 0 <![CDATA[Packaging Operator]]> Packaging Operator

Help Deliver Life-Changing Therapies Start Your Career in Pharmaceutical Manufacturing!

Location: Miami, FL
Industry: Pharmaceutical
Schedule: 5pm-5am week 1-Mon/Tues/Wed/Thurs, week 2 Mon/Tues/Wed with training up to 3 months M-F, 5am-1:30pm or 1pm-9:30pm or 9pm-5:30am
Salary: $17.50/hr. plus 12% shift diff which is $19.60/hr.).
Employment Type: Contract with the opportunity to go permanently based on performance and business needs. Multiple openings!

Overview: Are you looking for a stable, purpose-driven role where your work truly makes a difference? Join a dynamic pharmaceutical team at the forefront of innovation in mental health and women s health. As a Packaging Operator, you ll play a vital role in producing life-saving transdermal therapies using advanced drug delivery technology trusted nationwide.
In this hands-on role, you ll support the end-to-end manufacturing and packaging process operating and maintaining production equipment, weighing and verifying raw materials, and ensuring products meet the highest standards of quality and safety. All work is performed in strict adherence to cGMP, SOPs, and safety protocols within a state-of-the-art pharmaceutical environment.

Responsibilities:

Operate, clean, and maintain production and packaging equipment in a cGMP-compliant environment
Measure, weigh, and verify materials to ensure product accuracy
Support end-to-end production processes including manufacturing, pouching, labeling, and packaging
Set up equipment for clinical study packaging runs and batch production
Maintain detailed records and follow SOPs to ensure safety and compliance
Pitch in with shipping, receiving, and warehousing tasks as needed

Qualifications:

A high school diploma (or equivalent).
Experience with packaging in any setting - distribution, warehouse, or manufacturing. (No prior pharmaceutical or GMP/FDA experience required!)
Willingness and ability to learn new processes quickly.
Strong attention to detail and good communication skills.
Comfort using basic computer programs like Outlook.
Ability to thrive in a hands-on production environment where you may be exposed to moving parts, airborne particles, and some odors.

Why Join Us:

Work-Life Balance Enjoy four 10-hour shifts (Monday Thursday) with optional overtime on Fridays and Saturdays.
Career Growth This is a contract role with strong potential for permanent hire based on your performance.
Mission-Driven Culture Be part of a diverse, inclusive workplace focused on patient care, quality, and innovation.
State-of-the-Art Facility Join a highly regulated, FDA- and DEA-approved manufacturing site producing millions of patches each year.
Advancement Opportunities Learn, grow, and build a long-term career in the pharmaceutical industry.

Ready to join a company that s making a real difference in people s lives? Apply today and help deliver therapies that matter.
SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model partnering closely with clients to understand not only the role, but the company s culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.

EOE/ADA
IND123

]]> Tue, 13 Oct 2026 00:00:00 EDT 0 <![CDATA[QA Inspector]]> QA Inspector
SRG4 offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Location: Kendall, Florida
Industry: Pharmaceutical
Hours: Monday-Thursday, 2^nd shift, 3:30pm-2:00am
Salary: $20/hr. with 10% shift differential
Employment Type: Contract with the opportunity to go permanently based on performance and business needs.

Environment: Our client is a dynamic specialty pharmaceutical company engaged in the research, development, manufacture, marketing, and sale of prescription pharmaceutical products. They are a leading developer of advanced transdermal drug delivery technologies and prescription transdermal products.

Overview
Perform Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP s, Safety initiatives, Company policies, FDA and DEA regulations. Document all work performed, ensuring accuracy and thoroughness. Inform management of any deviations from established standards/procedures.

Responsibilities

Inspect and approve rooms, lines and equipment prior to use by manufacturing and R&D personnel.
Approve components for in-process operations.
Monitor manufacturing areas for compliance with internal SOPs, cGMPs and FDA/DEA regulations.
Document all work activity in appropriate batch records, forms, and logs to ensure accuracy and compliance.
Sample in-process items and finished products. Perform required inspections and testing of in-process items and finished products. Process and distribute samples to different departments.
Review records for cGMP compliance for accuracy and thoroughness.
Inform management of problems, failures and deviations from established internal and regulatory standards.
Apply disposition sticker to components and in-process materials.
Issue QA Alerts whenever any questionable component, in-process material or product is identified at any stage of production or storage.
Perform swab and Rodac Plate sampling as required.
Perform transactions in JD Edwards when required.

Qualifications

High school diploma or equivalent. Basic computer skills required. Basic math skills required (i.e., calculating %, addition, subtraction, multiplication, division). Ability to read, write, communicate and follow instructions (verbal and written) in English is required.
JD Edwards experience preferred, but not required
Minimum 1-2 years within an FDA/cGMP environment inspecting products

Keywords: inspections, inspector, quality, QA, batch records review, manufacturing, production, documentation, in-process, sampling, cGMP, GMP, FDA, pharmaceuticals, finished products

EOE/ADA

]]> Thu, 08 Oct 2026 00:00:00 EDT 0 <![CDATA[Manufacturing Operator]]> Manufacturing Operator

Location: Miami, Florida
Industry: Pharmaceutical
Hours: 5am-5pm with rotating schedule. Week one is Friday, Saturday, Sunday and week two is Thursday, Friday, Saturday and Sunday. OT and weekends required. Training schedule is M-F 5:00 am - 1:30 pm / M-F1pm-9:30pm / M-F, 9pm-5:30am up to 3 months until team is ready to transition to shift.
Salary: $19.50/hr. plus 10% shift differential ($21.45/hr.)
Employment Type: Contract with the opportunity to go permanently based on performance and business needs. (multiple openings)

Operate punching, pouching and cartooning machines.
Operate blending, coating, and slitting machines.
Blend various ingredients for the coating process.
Perform set-ups and operate the equipment in the prescribed area of responsibility.
Assure work center operates safely to produce products within established quality standards within the cGMP and SOP guidelines.
Check and weigh components to ensure compliance.
Clean production room and equipment.
Perform duties as trained and assigned.
Maintain a clean organized work area.
Ability to follow oral and written instructions.
Ability to work in a fast-paced manufacturing environment.
Must meet medical requirements for personal protective equipment (PPE) used in manufacturing.
Ability to work with Controlled Substances and all required procedures.
Completes assigned training curriculums within assigned time frames before performing any activity associated with the training topic.
Ensure documentation is completed and meet the prescribed standards.

Education / Experience:

High school diploma. Candidate must demonstrate mechanical aptitude, ability to speak, read and write in the English language and demonstrate the ability to perform basic mathematical calculations.
Knowledge and experience with Outlook and basic computer proficiency in how to navigate computers.

Judgment / Decision Making:

Ability to ascertain that work complies with approved standards and meets the prescribed guidelines. Must be able to operate production equipment with minimal supervision from the LMO. Employee must demonstrate the ability of adhering to stringent documentation requirements.

Work Environment:

Plant floor, pharmaceutical products.

Physical Demands:

The employee is occasionally required to climb, balance, stoop, kneel, and crouch. Must demonstrate the ability to lift and or move 50 pounds or greater.

Location: Kendall, Florida
Industry: Pharmaceutical
Hours: 5am-5pm, week 1-Fri/Sat/Sun, week 2-Thurs/Fri/Sat/Sun, plus OT when needed. 5pm-5am, week 1-Fri/Sat/Sun, week 2-Thurs/Fri/Sat/Sun, plus OT when needed. Training schedule options for up to 3 months 1st shift, M-F 5am-1:30pm, 2nd shift, M-F 1pm-9:30pm or 3rd shift, M-F 9pm-5:30pm
Salary: $20/hr. with 10% or 15% shift differential depending on assigned shift
Employment Type: Contract with the opportunity to go permanently based on performance and business needs.

Environment: Our client is a dynamic specialty pharmaceutical company engaged in the research, development, manufacture, marketing, and sale of prescription pharmaceutical products. They are a leading developer of advanced transdermal drug delivery technologies and prescription transdermal products.

Overview
Perform Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP s, Safety initiatives, Company policies, FDA and DEA regulations. Document all work performed, ensuring accuracy and thoroughness. Inform management of any deviations from established standards/procedures.

Responsibilities

Inspect and approve rooms, lines and equipment prior to use by manufacturing and R&D personnel.
Approve components for in-process operations.
Monitor manufacturing areas for compliance with internal SOPs, cGMPs and FDA/DEA regulations.
Document all work activity in appropriate batch records, forms, and logs to ensure accuracy and compliance.
Sample in-process items and finished products. Perform required inspections and testing of in-process items and finished products. Process and distribute samples to different departments.
Review records for cGMP compliance for accuracy and thoroughness.
Inform management of problems, failures and deviations from established internal and regulatory standards.
Apply disposition sticker to components and in-process materials.
Issue QA Alerts whenever any questionable component, in-process material or product is identified at any stage of production or storage.
Perform swab and Rodac Plate sampling as required.
Perform transactions in JD Edwards when required.

Qualifications

High school diploma or equivalent. Basic computer skills required. Basic math skills required (i.e., calculating %, addition, subtraction, multiplication, division). Ability to read, write, communicate and follow instructions (verbal and written) in English is required.
JD Edwards experience preferred, but not required
Minimum 1-2 years within an FDA/cGMP environment inspecting products