Annandale Science & Technology Job Listings

Lab Operations Associate63851107910275120

Workable

Lab Operations Associate

SOKOL GxP Services is seeking a Lab Operations Associate to support our client’s CPD Laboratory Operations team in New Brunswick, NJ. In this role, you will be responsible for the installation, setup, and troubleshooting of new laboratory equipment, while also assisting with compound and inventory management activities. Key responsibilities include fulfilling compound requests, cataloging and labeling compounds, performing quality control checks on lab instrumentation, utilizing inventory management software, and completing sample management work orders. You will also deploy small laboratory equipment throughout the site to ensure smooth day-to-day operations. This is a 100% on-site position with a Monday–Friday schedule during normal business hours. The assignment duration is 4 months. Requirements Bachelor’s degree in physical, biological sciences, or engineering (required) 0–3 years of relevant laboratory experience Experience in compound management preferred; demonstrated competency in chemistry or biology lab work Familiarity with analytical balances and/or liquid handling instruments desired Strong problem-solving, oral, and written communication skills Ability to work independently as well as in a team environment Must have legal authorization to work in the U.S. (no sponsorship or C2C accepted) Benefits Competitive hourly rate: | $21.41 – $27.20/hour (W-2 only, no C2C) 4-month contract with possible extension Health benefits, holiday pay, and 401(k) program Paid time off (UTO) and professional development support Employee referral bonus program Opportunity to contribute to high-impact projects with a leading biopharma company

New Brunswick, NJ, USA

$21-27/hour

Research Insights Co-Op63845341229187121

Workable

Research Insights Co-Op

Are you fascinated by what makes people tick? Are you able to get people to open up and share? Do you see patterns that other people don’t? Does research data “pop” for you, making it easy to separate what’s important and get to the bottom of what people are really saying? If your answer is yes, this is a role where you can positively impact millions of patients. The Insights Co-Op assists with patient-centric research studies and workshops for medical device development. They engage directly with patient and healthcare worker study participants, bringing creativity and empathy to their work. The Co-op has frequent interactions with the cross-functional Matchstick team of engineers, clinicians, and designers. Based on the project assigned, there is the opportunity to participate in pharmaceutical client meetings. This role is designed for a 5-8 month duration. ABOUT MATCHSTICK We are a consultancy working in chronic disease, specialty pharmaceuticals, and digital health. Much of our work focuses on combination products (medicine in a delivery device) like inhalers and injectors. Our work is diverse – from user research to understand what people need their devices to do, to creatively thinking about new designs and features, to helping our clients build business cases for development projects. Our clients are pharma and medical device manufacturers of all sizes. We invent, test, refine, and commercialize better solutions to help patients and health care practitioners. Our team is intentionally small and recognized by our pharma clients as being the best at what we do. Small but mighty, we dominate the early concept phase of this work. We are engineers, clinicians, designers, and businesspeople. Each project is at the forefront of chronic disease treatment – we get given the very toughest questions, and there is no “right” answer or cookie-cutter process. We are based in Boonton, NJ in the center of town at the former Boonton Opera House. Team members are generally in-person 3 days per week and to support occasional events (workshops, client visits, etc.). RESPONSIBILITIES Help facilitate qualitative study interviews including prototype handling, session recording, and data collection. Create research materials (study stimuli, kits, surveys, screeners, etc.). Analyze and organize results to extract findings. Use qualitative techniques including task analysis, thematic analysis, and similar. Perform and interpret quantitative statistical analyses. Contribute to narrative around research results. Help present results that communicate insights and implications for our clients. Present regular updates to internal team and the client to ensure client needs are met and changes are incorporated. Participate in creative brainstorms for new medical devices, features, or functionality. Research topics of interest to us (e.g. rare disease states, new pharmaceuticals, etc. ) using academic research, blogs, and social media. Teach the team what you've learned, and extract a clear "so what". Practice core consulting skills that will enable you to frame problems effectively, write clearly, present confidently, and facilitate fast and effective team meetings. Get regular feedback and coaching around your work (the "what") as well as your style (the "how"). Requirements WHO YOU ARE We encourage you to bring your unique talents to this role. As a small team, we find enthusiasm, mindset, and experience to be more important than degrees. Based on our experience, you are a good candidate if: You are currently pursuing a Bachelor’s or Master’s degree in one of the following fields: Biochemistry/Biophysics, Biology, Biomedical Engineering, Chemical Engineering, Industrial Engineering, Biotechnology, Cognitive Science, Psychology, or Design Innovation. Minimum status of Sophomore in a Bachelor's degree program. You are naturally curious. You're a quick learner and you enjoy doing so. You are a problem solver. You are energized by complex challenges and are solutions focused. You love working directly with patients, caregivers, and clinicians. You find passion in empowering people to manage disease. You could not imagine working on anything more important. You're interested in other people and what makes them tick. You quickly understand where others are coming from. You make people feel heard, valued, and respected in every interaction. You love the details, but don't get bogged down in them. You know that 20% of the information you discover is really important, and know how to focus on and communicate what matters. You are entirely comfortable with ambiguity and not having a clear answer. You have no problem walking into an unfamiliar situation, getting your bearings quickly, and working with others to find a solution. You are honest and forthright. We work in a regulated industry and we despise passive aggressiveness and other bad corporate behavior. You are available to work full time (40 hours per week), during standard business hours. You are authorized to work in the US. We cannot sponsor any authorizations. EXPERIENCES THAT WILL PUT YOUR RESUME ON TOP These are not requirements for the role, but we’re always interested in specific skill sets and experiences that are a good fit for our work. Medical device or healthcare experience. Hands-on experience with creating study designs and design of experiments (DoE). Experience with human-subjects research in social science fields. Familiarity with usability assessments, contextual inquiry, human factors, or other formal research techniques. Familiarity with journey mapping, co-creation, and other human-centered design approaches. Demonstrated experience with secondary research and synthesis. Interest in sustainable design and manufacturing. Published writing in academic papers, school newspapers, or similar. Familiarity with quantitative data analysis tools e.g. R, python, SPSS, Prism

Boonton, NJ 07005, USA

Negotiable Salary

Environmental Chemist – Big $ Weekends – Green Jobs – No Exp Necessary (North Jersey)63580736586115122

Craigslist

Environmental Chemist – Big $ Weekends – Green Jobs – No Exp Necessary (North Jersey)

Regional Environmental Company looking for hard-working individuals to work at local household hazardous waste events (HHW). Mostly Saturdays. Hours vary but are generally 6:30am to 3:30pm. LOCATIONS VARY EVERY WEEKEND. We do events for Bergen County, Middlesex County, Essex County, Morris County, Sussex County, Warren County, Hunterdon County, Mercer County, Camden County, Passaic County, Gloucester County, Atlantic County, Cape May County, and Cumberland County. We also do events around Philadelphia, Eastern Pennsylvania, Connecticut, Massachusetts, New Hampshire, Upstate New York, and Long Island. No experience necessary. Check out this video to find out who we are and see what the job is like! Copy and past this link https://www.youtube.com/watch?v=JA_41Mibavg Or YouTube search for video titled “MXI HHW - Household Hazardous Waste Events” HHWs are events sponsored by the local waste authorities that provide residents a place to drop off their household hazardous waste for proper disposal such as paint, oil, gas/thinners, pesticides, cleaners, pool chemicals, aerosol cans, propane, bulbs, batteries, etc. Our company, MXI Environmental Services, is a private company that bids on managing these events. We provide trucks, equipment, and staff to manage the collection of the waste, characterize it, pack it in proper UN rate containers, and load it to ship into permitted trucks. LOCATIONS VARY EVERY WEEKEND. Events take place on Saturdays and some Sundays. Hours vary but are generally 6:30am to 3:30pm. Pay begins at $275 for the day for qualified candidates and can grow up to $350 per day with additional training and responsibilities. Those Candidates without qualifications are eligible for hire and start at $200. Increases happen quickly if you show up, work hard, and are nice. We like to aggressively keep good people. Additional increase come with good attendance, hard work, and more responsibilities/skills. Experience with a forklift is a plus. To qualify for $275 starting pay you need: • Bachelor’s Degree in Applied Science (Biology, Chemistry, Environmental Science, ect.) from an accredited college/university located in the United States • Or a CURRENT 40 Hour HAZWOPER training certificate. Must provide copy of degree and official transcripts/ CURRENT 40 Hour HAZWOPER training certificate to qualify. Good clean cell phone pictures will suffice but we need verification. Foreign degrees or Science degrees in not applicable fields (eg. Psychology, Business Administration) will be evaluated on a case by case basis. Upon completion of training New Chemist Candidates will be assigned 3 jobs for an introductory evaluation. You would initially start the same as all new staff and be responsible for safely unloading waste from citizens' cars and safely transporting it to a sortation area occupied by highly trained staff. All staff also helps setup and clean up after the event. After three events you will begin to learn additional skills and assigned additional responsibilities in line with your educational background and performance. With good attendance, attitude, and performance, you will begin field training with a qualified Field Chemist at the events and begin training for the next step. After the first 3 jobs, the candidates will be given a schedule of work for the immediate future and remainder of the season. Staff is expected to be available on Saturdays. Particularly in the Spring and Fall. Throughout the year we understand if there are a few weekends you need off for important events, such as weddings, family vacation, ect. With proper notice that’s no problem. But we want to make clear this is a weekend job and want people who want to work consistently on the weekends. New staff would be required to complete an online company training seminar before working the event. The company provides an extra $25 in the first paycheck as compensation for the training. No experience in the Environmental field is necessary. Best asset for candidates is a strong work ethic. The company values and rewards hard work. Those who do not work hard will not be invited back to work regardless of past experience or credentials. Most work opportunities are local however some weekends the opportunities require travel. The company coordinates and sponsors travel those interested. Travel is not required and you can clarify if you only want local in the application process. Those who travel are rewarded on the slow weekends with first dibs. Required: • Transportation to and from the job • Complete online training (will receive $25 in first paycheck for training) • Jeans and hard toe work boots onsite (company provides shirt and all other personal protective equipment) • Ability to lift 40lb repeatedly • Ability to be on feet for better part of 8 hours • Good work ethic and a great attitude Benefits: • Pay increase to as much as $350 per event • Breakfast, lunch, and drinks provided on the job • Recruiting bonuses for signing up friends and associates to work with you • Excellent resume experience • Will provide letters of recommendation for hard working individuals we invite back! They are an excellent tool for future job interviews. For more information on the company and the events please check out our website at www.mxiinc.com and this video we put up on youtube! https://www.youtube.com/watch?v=JA_41Mibavg IF YOU ARE INTERESTED PLEASE RESPOND TO THIS ADVERTISMENT WITH THE FOLLOWING INFORMATION: • FULL NAME • EMAIL ADDRESS • PHONE NUMBER • A brief summary about yourself Please attach a resume if available. Incomplete responses will be discarded. FAQs • Where are the events? Locations vary every weekend. • Does the company provide transportation? For local and in state jobs the company does not. You are expected to transport yourself. There are travel bonuses for some jobs depending on distance. For out of state jobs, or long rides, the company has provided travel bonuses on a case to case basis. • How do we pay? With a hard check same day at the end of the event. If you live in NJ, then you come on an employee and get paid via direct deposit the following Friday (6 days after most events). • How do you get to $350 per day? That is the rate for the Lead Chemist. You need at least 1 job as the Lead with a Field Chemist. This usually happens over a year. You must be trained on all job functions and prove you are reliable. It does not happen overnight but we will train the best candidate.

624 Hillside Ave, Boonton, NJ 07005, USA

$200-350/day

Packaging Operator (Contract to Hire) (Monroe)63582422306689123

Craigslist

Packaging Operator (Contract to Hire) (Monroe)

If interested, please reply with a copy of your resume. Thank you! SUMMARY We are looking for a Packaging Operator to join our production team. This position involves running and maintaining packaging machines, ensuring that products are prepared accurately and efficiently while meeting quality and safety standards. The role is ideal for someone with mechanical skills, attention to detail, and a strong interest in working within a structured manufacturing environment. RESPONSIBILITIES • Set up, operate, and oversee packaging equipment to keep production running smoothly. • Perform routine checks and address mechanical problems to minimize downtime. • Ensure all tasks are carried out in compliance with FDA regulations and Good Manufacturing Practices (GMP). • Work with team members to assemble and package products for distribution. • Record production data clearly for quality and tracking purposes. • Keep the workspace organized, sanitized, and in compliance with safety procedures. QUALIFICATIONS • Previous experience in a packaging or manufacturing environment preferred. • Mechanical aptitude with the ability to troubleshoot equipment. • Knowledge of FDA and GMP quality requirements. • Exposure to programmable logic controllers (PLCs) a plus. • Experience in assembly operations is an advantage. • High attention to detail to ensure correct labeling and quality output. • Able to lift up to 50 lbs. as part of daily tasks. • Proficient in reading, writing, and understanding English.

48-50 Station Rd, Cranbury, NJ 08512, USA

$18/hour

QA Associate (Temp) (Stanhope, NJ)63582364944513124

Craigslist

QA Associate (Temp) (Stanhope, NJ)

If interested, please reply with a copy of your resume. Thanks! SUMMARY This position supports essential Quality Assurance functions in a growing pharmaceutical organization. It involves maintaining documentation, assisting with compliance, supporting inspection readiness, and performing administrative tasks to ensure regulatory and internal quality standards are met. RESPONSIBILITIES • Keep current knowledge of standard operating procedures (SOPs). • Assist in delivering training initiatives across multiple teams. • Review quality assurance and quality control documentation, including logbooks. • Maintain and organize documentation systems accurately. • Input data into quality tracking databases and systems. • Support cleanroom and laboratory sanitation practices per cGLP guidelines. • Provide supporting documentation for audits and inspections. • Manage documentation issuance, tracking, and secure storage. • Oversee label issuance and participate in label counting and verification. • Ensure company and regulatory compliance is upheld across operations. • Follow all applicable current Good Manufacturing Practices (cGMP) including those in the FD&C Act Section 503B. • Support document control practices and monitor data for quality trends. • Carry out additional duties as needed to support Quality initiatives. QUALIFICATIONS • Associate degree preferred. • 2–5 years of experience in pharmaceutical or related field, or an equivalent blend of education and experience. • Strong attention to detail with excellent organization skills. • Experience using spreadsheets and databases. • Ability to manage shifting priorities and work on multiple tasks daily. • Positive team-oriented mindset with strong communication skills. • Must maintain confidentiality of sensitive information.

11 Nalron Dr, Ledgewood, NJ 07852, USA

$25/hour

Workable

General Manager, US

About VCLS Voisin Consulting Life Sciences (VCLS) is the global reference partner accelerating HealthTech products’ access to regulated markets. From discovery to patients, VCLS provides end-to-end HealthTech solutions that support biotech, pharmaceutical, and medical device companies throughout product development and the entire lifecycle. Our integrated services span clinical research, vigilance, regulatory strategy and submissions, chemistry manufacturing and controls (CMC), and market access. With 230+ life science professionals across 10 countries and 4 continents, VCLS partners with a broad range of innovators and investors to bring transformative HealthTech solutions worldwide. The US market is central to VCLS’s global ambitions and is a critical focus for our future growth. Role Overview As General Manager, US, you will lead VCLS’s Life Sciences consulting business across North America, driving strategic growth, operational excellence, and high-level client engagement. In this role, you will own the business and financial performance of the US entity, VCLS Inc., and be expected to generate business that contributes to the success of the entire company. You will partner closely with global senior leadership and collaborate cross-functionally to achieve ambitious goals. This opportunity is ideal for an executive with exceptional sales and networking capabilities, with experience opening doors at the C-suite level in Biotech, Pharma, MedTech, and the investment community, and building relationships that translate into meaningful business. You are an inspiring leader who can grow, develop, and engage the US team in close partnership with functional leaders, fostering a strong culture, high utilization, and consistent professional development. Key Responsibilities Market Leadership & Strategic Growth Define the strategic vision and market positioning for VCLS services in the US and lead the execution of a market strategy aligned with our global objectives. Drive high-level business development build and sustain relationships with senior leaders, innovators, and investors. Position VCLS as the preferred partner across regulatory, clinical, and development services. Proactively generate global business opportunities originating from the US market. Operational & Financial Management Hold full accountability for the financial performance of the US business, ensuring sustainable growth and profitability. Oversee project delivery and service quality, maintaining compliance and exceptional client satisfaction. Collaborate with global functional leaders to optimize resource allocation, maximize utilization, and avoid duplication of expertise. Team Leadership & Talent Development Lead US-based consulting and business development teams, fostering a culture that reflects our PIPE values: People, Innovation, Passion, Excellence. In partnership with global and functional leadership, hire, set objectives, coach, develop, and monitor the performance of employees. Partner with HR and functional managers to drive engagement, career growth, and retention. Ensure employees are effectively integrated into global teams. Champion a collaborative, high-performance environment. Requirements Qualifications Senior leader with a proven track record in Life Sciences consulting, regulatory strategy, clinical development, or adjacent fields. Demonstrated success in business development and strategic client acquisition at the C-suite level. Well-established network within US Biotech, MedTech, Pharma, and investment communities. Strategic thinker capable of shaping market positioning and growth strategy. Inspirational people leader who has built, coached, and retained high-performing teams in global, matrixed organizations. Strong financial acumen with prior P&L accountability. Excellent communication and influencing skills, with the presence and credibility to represent VCLS externally. Entrepreneurial mindset with a collaborative, solutions-focused approach. Advanced degree in Life Sciences, Medicine, Pharmacy, or a related discipline; MBA or business qualifications are a plus. Benefits What We Offer The opportunity to lead a strategically critical business in one of the most dynamic life sciences markets in the world. A collaborative global culture grounded in scientific excellence and client partnership. Direct engagement with global senior leadership. Competitive compensation, performance-based incentives, and significant career growth potential. Join Us If you are an agile, entrepreneurial leader with a passion for Life Sciences consulting, a commitment to excellence, and the ambition to build a high-growth US business, we invite you to explore this opportunity with VCLS.

Somerville, NJ 08876, USA

Negotiable Salary