Regulatory Assistant - Chemicals Job at SRG (Manchester)

Research Assistant Bioanalytical

Research Assistant Bioanalytical Pharmacokinetic (PK) research. Position is in a...

Location

United States , Greenfield

Salary:

24.00 - 28.00 USD / Hour

Labcorp

Expiration Date

Until further notice

Requirements

Bachelor's degree (BS/BA) in Chemistry or a related scientific field
6 months or more of LC‑MS experience
6 months or more operating, calibrating, and troubleshooting quadrupole LC-MS
1 year or more of experience with standard laboratory equipment (balances, pipettes, centrifuges)
1 year or more of HPLC experience
Ability to start working full-time in the next 2-8 weeks
Comfort working in high production scientific lab
Comfortable working with samples from Animal Research

Job Responsibility

Analyze biological or chemical samples for various compounds in compliance with SOPs and regulatory guidelines
Compile and report results to management
Organize, conduct, and evaluate analytical testing and results
Maintain study documentation and laboratory records
Set up, operate, and maintain general laboratory equipment, including troubleshooting and resolving issues
Perform quality control reviews of data
Communicate deviations or issues that may affect data integrity to the Study Director, Principal Investigator, or management, and participate in corrective actions
Assist with method development and validation for various analytes across multiple matrices
Perform complex analyses using new or unfamiliar methods, seeking scientific guidance when needed
Recommend improvements to test methods or procedures

What we offer

Medical
Dental
Vision
Life
STD/LTD
401(k)
Paid Time Off (PTO) or Flexible Time Off (FTO)
Tuition Reimbursement
Employee Stock Purchase Plan

Fulltime

Manufacturing Engineer – Industrial & Metallurgical Processes

The Manufacturing Engineer will play a critical role in driving operational exce...

Location

United States , Huntsville

Salary:

Not provided

Kennametal

Expiration Date

Until further notice

Requirements

Bachelor's degree in Manufacturing Engineering, Industrial Engineering, or a related discipline
Experience supporting manufacturing processes in an industrial or process-based environment
Strong knowledge of process improvement methodologies, Lean manufacturing, and operational excellence principles
Working knowledge of statistical analysis and process control tools
Proven problem-solving and root cause analysis skills
Experience with metallurgical or chemical process manufacturing
Experience leading or supporting capital equipment projects
Familiarity with furnace operations, chemical processing, material blending, or screening processes
Lean Six Sigma certification (Green Belt or higher)
Must be legally authorized to work in the US (excluding Optional Practice Testing) and not require sponsorship now or in the future

Job Responsibility

Develop, evaluate, improve, and document metallurgical and manufacturing processes to ensure consistent quality, safety, and performance
Provide daily engineering technical support for manufacturing operations, including furnace room, chemical plant, blending, and screening areas
Troubleshoot and resolve technical and process-related issues to minimize downtime and defects
Monitor process controls and ensure adherence to established standards and specifications
Analyze process flow and manufacturing data to improve product quality, cost reduction, throughput, and first-pass yield
Identify process deficiencies and lead the development and implementation of corrective and preventive actions
Apply Lean manufacturing and continuous improvement principles to eliminate waste and improve overall equipment and process effectiveness
Utilize statistical methods (SPC, process capability analysis, repeatability and reproducibility studies) to improve process performance and conformance to quality requirements
Lead and support capital projects, including equipment design, procurement, installation, commissioning, and validation
Assist in the design and layout of processes, machinery, and material flow to optimize efficiency, safety, and ergonomics

Fulltime

Field Measurement Specialty Operator

Our major client is seeking a Field Measurement Specialty Operator to work withi...

Location

United States , Houma

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

High School Diploma or Equivalent
Valid Driver's License
Must be capable of physical duties in outdoor environment

Job Responsibility

Sales Measurement Witnessing for Gas and LACT Oil Custody Transfer including gas calibrations, gas chromatography, LACT meter provings, sampling for quality and quantity determination with associated documentation administration
Allocation measurement duties including conducting gas calibrations of Sr. Orifice fittings, review of 3rd party oil and condensate meter calibrations, administration of allocation sampling for both composite and spot sampling in accordance with API Standards and industry best practices, interface with I&E personnel for measurement device data flow into Delta V supervisory system
Well Measurement and Testing duties including validation of well testing for allocation purposes, S&W determination for well testing via Red Eye Water Cut Meter and actual sampling for S&W determination via Shake-out as necessary, calculation review of Multiphase Flow Meter exception testing for subsea field allocation into overall Devils Tower allocation
Regulatory Compliance Administration including tracking BSEE compliance for sales meter provings, run tickets, security sealing logs, prover water draw certifications and associated Surface Commingling & Production Measurement Permit compliance
Monitor chemical injection rates
Monitoring levels in vessels, flushing bridals as directed by control room
Compliance testing safety systems
Rigging for crane operator during crane activities
Opening and closing manual valves, as directed by the control room
Assist in platform maintenance, washing decks and cleaning facility

Fulltime

Research Associate I, R&D Complex Product Development

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience in SEC-UV-MALS and related methods encompassing liquid chromatography, light scattering, diffraction and light obscuration
Competency in the acquisition, processing and data analysis by SEC-UV-MALS and light scattering/diffraction/obscuration techniques for analysis of peptides and iron colloidal products for regulatory submissions is mandatory
Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
Basic understanding of working principles of biophysical & spectroscopic methods, like CD, FTIR, UV, EPR, Mossbauer, and fluorescence spectroscopy, particle XRD, microscopy methods (AFM & EM) & related orthogonal methods to assess structural properties of proteins and iron colloids
Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
Trouble shooting of various problems obtain during the product development
Knowledge of good laboratory practices and good documentation practices
Communication skills

Job Responsibility

To perform advanced characterization of complex injectable drugs, including iron formulations, proteins & peptides, oligonucleotides, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation. Traveling to external facilities, as and when required, is a mandatory requirement for this position
To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
To understand the project with guidance of Sub-department Manager and follow their instructions
To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia. Data recording in ELN and sign off must be completed on time
To verify the shelf life of the chemical or reagent before performing analysis of the material or product
To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Regulatory Compliance Manager

The Regulatory Compliance Manager oversees the product-related regulatory compli...

Location

United States , Malvern

Salary:

10000.00 - 13000.00 USD / Year

Beacon Hill

Expiration Date

Until further notice

Requirements

Bachelor's degree in scientific discipline such as Chemistry, Biology, Microbiology, Physics, Quality, or Environmental Science
At least 5-8 years of experience with regulations, SOPs, compliance, and/or quality management in pharmaceutical, biotech, medical, medical product, hygiene, cleanroom engineering/products manufacturing, or other regulated chemical industry
Knowledgeable in domestic and international chemicals
Communicates clearly, professionally and concisely, both verbally and in writing
Proficiency with Microsoft Word, Excel, and PowerPoint are required
Exceptional attention to detail and organizational skills
Ability to manage multiple projects and competing priorities

Job Responsibility

Serves as a subject matter expert for chemical, disinfectant, and antimicrobial products
Develops and implements global regulatory strategies to support product commercialization, lifecycle management, and market expansion
Reviews and monitors regulations with respect to global activities
Prepares summaries of new and changing regulatory requirements and communicates potential impacts as necessary to senior management
Provides regulatory input during product development, formulation changes, and manufacturing changes to assess regulatory impact and approval requirements
Coordinates product registration at domestic and international levels
Prepares regulatory submissions prior to agency filing
Domestic regulatory activities, including EPA and FDA annual volume reporting, as well as product and establishment renewal activities, and US State registrations and renewals
Responds to regulatory agency inquiries connected to registrations, notifications and changes
Participates in audits and inspections performed by regulatory agencies and prepares supporting and briefing documents as necessary

Fulltime

Facility Engineer – Wastewater Treatment Plant

In a Wastewater Treatment Plant environment you will be responsible for the effe...

Location

United States , Wyandotte

Salary:

Not provided

Veolia

Expiration Date

Until further notice

Requirements

B.S. in Civil, Chemical, or Mechanical Engineering is preferred
Three (3) years of experience
Valid Driver License

Job Responsibility

Define engineering project scope, receives and analyzes bid proposals, develops and writes PERs and CERs, develops conceptual designs including detailed drawings, written project descriptions, time and financial estimates, and project justifications
Meet with vendors and contractors to provide direction in planning and construction of required operational and engineering opportunities in accordance with material specifications, drawings, project scheduling, and safety, health, and permit considerations
Track and controls monetary expenditures and physical progress of assigned projects. Approves personnel time sheets, equipment usage charges, materials/supplies, and invoices
Manage regulatory inspection projects and associated documentation for storage tanks and boilers
Manages Maintenance Department
Work with Operations and Maintenance in identifying, analyzing, and resolving various engineering projects
Ensure that all applicable safety and environmental regulations are followed during the performance of all job tasks
Assist in coordinating and supervising contract job activities
Other duties as assigned

What we offer

Paid time off policies
health
dental
vision
life insurance
savings accounts
tuition reimbursement
paid volunteering
employer sponsored 401(k) plan

Fulltime

Medical Laboratory Scientist

Performs and reports waived, moderately complex, and highly complex test procedu...

Location

United States , Madisonville

Salary:

28.67 - 42.64 USD / Hour

American Nursing Care

Expiration Date

July 16, 2026

Requirements

Bachelor's degree in Medical Technology, biology, or chemical science.

Job Responsibility

Performs and reports waived, moderately complex, and highly complex test procedures on patient specimens adhering to the Section's Standard Operating Procedures to ensure accurate and timely reporting
Provides excellent patient care through clinical correlation of results, identification of patterns of bias, rapid notification of appropriate caregivers of critical values, and completion of testing within established turn-around-time limits
Ensures that major automated equipment is operational by performing required maintenance, calibration and troubleshooting procedures
including contacting of instrument vendor for assistance or repair
Performs required calibration and quality control procedures and maintains records to ensure tests are being performed within established parameters
Performs proficiency testing as assigned and review results with laboratory clinical leaders
Assists in evaluation and generation of compliant documentation for the validation of new procedures and equipment to provide the physician with the most current laboratory technology
Participates in opportunities for continuing education and/or teaching, training according to the Section Performance Standards to enhance technical skills of students, trainees, coworkers, and self
Responsible for inventory of supplies, including providing assistance with monitoring supplies, ordering, and placing received supplies into storage
Completes all work and resolves or appropriately passes ongoing issues to incoming staff within the scheduled shift

What we offer

medical
prescription drug
dental
vision plans
life insurance
paid time off
tuition reimbursement
retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings

Fulltime

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Assistant Production Manager

Our client is a well-established, medium-to-large-scale food manufacturing facil...

Location

Canada , Edmonton

Salary:

Not provided

Randstad

Expiration Date

August 27, 2026

Requirements

A minimum of 8 years of experience working within a medium to large-scale food manufacturing environment
Extensive hands-on experience operating and troubleshooting industrial manufacturing equipment, specifically industrial mixers and large commercial ovens
A strong background in baking with a functional understanding of ingredient functionality and process flows is highly preferred
Formal training in the Science of Baking, Leadership, or OHS is a significant asset
Deep knowledge of risk assessments, hazard principles (Biological, Chemical, Physical), and BRC/HACCP compliance standards
Exceptional time management, organizational skills, and a proven track record of motivating teams to meet established corporate goals
Intermediate proficiency with Microsoft Office Suite
Fluent in speaking, reading, and understanding English with strong documentation habits

Job Responsibility

Lead, mentor, and coach the supervisory team to build leadership capacity across the production floor
Manage and review staff scheduling to ensure timelines are consistently met
Partner daily with Shipping, Maintenance, Quality Control, and Sanitation managers to synchronize production outputs, manage equipment downtimes, and track inventory
Review Daily Efficiency Reports (labor, yields, scrap rates, and ingredient giveaway)
Investigate variances, conduct root-cause analyses for technical issues, and ensure all materials meet quality specifications
Enforce company rules, occupational health and safety (OHS) procedures, and regulatory standards (including BRC/HACCP)
Organize Toolbox Meetings, conduct hazard assessments, and assist in creating SOPs for new equipment
Monitor the tempering area for proper temperature specs and rotation
Maintain an organized, clean, and safe production floor by removing unused equipment

What we offer

Work-Life Balance: Enjoy a reliable Monday-to-Thursday shift structure
Tools Provided: Company-supplied cell phone
Apparel: Uniforms are fully supplied, alongside a safety shoe replacement program
Career Growth: A pivotal role with direct exposure to plant management and substantial leadership responsibilities

Fulltime

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Regulatory Assistant - Chemicals

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