What are the opening hours?

Monday 9am - 5:30pm Tuesday 9am - 5:30pm Wednesday 9am - 5:30pm Thursday 9am - 5:30pm Friday 9am - 5pm

Achieva, Achieva, Suite 1, Pilgrims Lodge, 1a Holywell Hill, Saint Albans (2026)

29/04/2025

💫 Direct Inhouse Manufacturer 💫

📍 Leicestershire

💼 Occupational Health Technician

🗓️ 3 days per week

📜 Permanent

💸 £25,000 - £30,000 per annum pro rata depending on experience.

👋 Get in touch with Abby for immediate consideration!

Said
📞 01727 817 636
📧 [email protected]

28/04/2025

🔹We're Hiring: Regulatory Affairs Specialist 🔹
𝐋𝐨𝐜𝐚𝐭𝐢𝐨𝐧: Zuchwill, Hybrid | 𝐒𝐭𝐚𝐫𝐭 𝐃𝐚𝐭𝐞: ASAP | 𝐃𝐮𝐫𝐚𝐭𝐢𝐨𝐧: Until December 31, 2025
𝐂𝐨𝐧𝐭𝐫𝐚𝐜𝐭 𝐓𝐲𝐩𝐞: Full-Time Contract | 𝐑𝐚𝐭𝐞: CHF 73.00 per hour

Are you passionate about navigating the regulatory landscape and ensuring innovative products reach markets compliantly?

We're looking for a Regulatory Affairs Specialist to join our Client's team and play a vital role in maintaining and expanding their product portfolio internationally!

🌟 𝐖𝐡𝐚𝐭 𝐘𝐨𝐮'𝐥𝐥 𝐃𝐨
As a Regulatory Affairs Specialist, you will:

● Lead the submission of licenses and authorizations for new and existing products.
● Support international registrations and manage product dossiers.
● Ensure regulatory conformance in product development, claims, labeling, and promotional materials.
● Provide strategic regulatory guidance to cross-functional product teams.
● Help develop best practices for Regulatory Affairs processes.
● Prepare and submit documentation to regulatory agencies and assist during internal and external audits.
● You'll have the opportunity to collaborate across teams, solve moderately complex challenges, and directly influence how innovative products are developed and brought to market.

🛠 𝐊𝐞𝐲 𝐐𝐮𝐚𝐥𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬

● Bachelor's degree (required).
● 2–4 years of regulatory affairs or related experience.
● Strong written and verbal communication skills.
● Excellent organizational and multitasking abilities.
● Experience with risk-benefit analysis techniques.
● RAC certification for Medical Devices is a strong plus!

✅ Why This Role?
This is an exciting opportunity to work on impactful projects, develop your regulatory expertise, and help bring transformative products to global markets.

📩 Interested? Apply now!
➡️ https://achieva.jobswith.us/ #/jobs/35892

𝐏𝐥𝐞𝐚𝐬𝐞 𝐍𝐨𝐭𝐞: 𝐓𝐡𝐞 𝐃𝐞𝐚𝐝𝐥𝐢𝐧𝐞 𝐟𝐨𝐫 𝐭𝐡𝐢𝐬 𝐫𝐨𝐥𝐞 𝐢𝐬 𝐓𝐮𝐞𝐬𝐝𝐚𝐲 𝟐𝟗.𝟎𝟒.𝟐𝟓 𝐛𝐲 𝟑𝐏𝐌 𝐂𝐄𝐓.

24/04/2025

🔍 We're Hiring: Quality Specialist
📍 Basel, Switzerland
📅 Start Date: ASAP | Contract: Initial 6-month contract with potential extension (Dependent on project requirements).
💼 Workload: Full-time (100%) | 💰 Pay: CHF 37.93–43.18/hour

Join our Client's team in Technical Research & Development and play a key role in ensuring GMP compliance for clinical supplies.

✨ What You'll Do:
✔️ Review batch records and GMP documentation
✔️ Support timely release of labels, primary packed materials & Investigational Medicinal Products
✔️ Maintain and archive QA-owned documentation
✔️ Contribute to process improvements and compliance initiatives
✔️ Collaborate cross-functionally with QA & GCS teams

📚 Your Background:
🎓 Technician or Bachelor's degree with 3+ years of experience
🗣 Fluent in German & proficient in English (oral & written)
🔬 Solid understanding of GMP, drug development & regulatory frameworks
🧠 Strong organisational skills and attention to detail

📈 Be part of a high-impact team driving excellence in pharmaceutical development!

👉 Apply now (https://achieva.jobswith.us/ #/jobs/35891) or tag someone who'd be a perfect fit!

22/04/2025

🚨 We're Hiring! 🚨
Looking for your next challenge in pharmaceutical logistics? Join our client as a Sample Management Officer!

We're hiring two roles – one full-time (100%) and one part-time (60%) – to support global sample and shipment processes in a GMP-regulated environment.

🔹 Start Date: ASAP
🔹 Contract: 12 months (with potential extension)
🔹 Pay Rate: 37.93 – 43.47 CHF/hour
🔹 Location: Basel Area, Switzerland (Hybrid)

What you'll be doing:
✅ Coordinating global shipments of pharmaceutical reference samples
✅ Sample preparation and inventory management (both digital and physical)
✅ Working hands-on with tools, systems, and cross-functional teams
✅ Ensuring compliance with GMP, GLP, and company quality standards

Who we're looking for:
🔍 3+ years' experience in global shipping logistics (GMP experience a big plus!)
🔍 Strong organizational skills and a hands-on, proactive mindset
🔍 Fluency in the English language (German proficiency is a bonus)

🎯 If you're detail-oriented, tech-savvy, and ready to make an impact — we'd love to hear from you!

👉 Apply now or learn more here: https://achieva.jobswith.us/ #/jobs/35890

Know someone who might be a great fit? Feel free to share or tag them below!

16/04/2025

We're Hiring: Senior Financial Analyst in Heerlen, Netherlands on a 6 Month Contract.

We are seeking a detail-oriented and analytical Financial Analyst to join our team with a primary focus on cost control and business support.

The ideal candidate will be responsible for monitoring financial performance, analysing cost drivers, and providing insights to support strategic decision-making.

This role requires strong financial modeling skills, business acumen, and the ability to collaborate with cross-functional teams.

📩 More details and how to apply here: https://achieva.jobswith.us/ #/jobs/35887

14/04/2025

🚨 𝐖𝐞'𝐫𝐞 𝐇𝐢𝐫𝐢𝐧𝐠! 𝐃𝐫𝐮𝐠 𝐒𝐚𝐟𝐞𝐭𝐲 𝐂𝐚𝐬𝐞 𝐌𝐚𝐧𝐚𝐠𝐞𝐫
📍 𝐋𝐨𝐜𝐚𝐭𝐢𝐨𝐧: Allschwil, Switzerland
🕰️ 𝐒𝐜𝐡𝐞𝐝𝐮𝐥𝐞: Full-time (100%)
📅 𝐒𝐭𝐚𝐫𝐭 𝐃𝐚𝐭𝐞: April/May 2025
📄 𝐃𝐮𝐫𝐚𝐭𝐢𝐨𝐧: 12 months
💰 𝐏𝐚𝐲 𝐑𝐚𝐭𝐞: CHF 73.72 per hour

Are you passionate about pharmacovigilance and ready to make a real impact in patient safety? Our Client are looking for an experienced 𝐃𝐫𝐮𝐠 𝐒𝐚𝐟𝐞𝐭𝐲 𝐂𝐚𝐬𝐞 𝐌𝐚𝐧𝐚𝐠𝐞𝐫 to join their team in Allschwil, Switzerland. If you thrive in a team-oriented environment and love the details that make a difference, this might be your perfect next move.

🔍 𝐘𝐨𝐮𝐫 𝐌𝐢𝐬𝐬𝐢𝐨𝐧
As a Drug Safety Case Manager, you'll play a vital role in processing adverse event (AE) reports in accordance with global regulations, SOPs, and guidelines. Your work will directly support patient safety and product excellence.

🧪 𝐖𝐡𝐚𝐭 𝐘𝐨𝐮'𝐥𝐥 𝐁𝐞 𝐃𝐨𝐢𝐧𝐠:
- Manage end-to-end AE case processing: triaging, data entry, AE coding, narrative writing, and submissions
- Prioritize cases to ensure timely regulatory reporting
- Collaborate with Drug Safety Physicians to request missing information
- Monitor workflows and case queues daily
- Oversee reconciliation activities

🎯 𝐖𝐡𝐚𝐭 𝐘𝐨𝐮 𝐁𝐫𝐢𝐧𝐠:
- Degree in Life Sciences (Pharmacy, Nursing, or similar)
- 5+ years of experience in safety or clinical data management
- Strong medical terminology knowledge and familiarity with disease processes
- Proficient in coding thesauri and drug dictionaries
- Deep understanding of EU & US safety reporting requirements
- Excellent organizational skills, team spirit, and calm under pressure
- Fluent in English (verbal & written)

👉 Ready to bring your expertise to a role that truly matters?
📩 Apply now (https://achieva.jobswith.us/ #/jobs/35882)
🤝 Connect with the PV Team to learn more!

🔁 Share this opportunity with your network.

14/04/2025

🚨 We're Hiring: Occupational Health Technician – South Sheffield (3 Days/Week) 🚨

Achieva is proud to be partnering with a leading manufacturer to recruit for a permanent in-house Occupational Health Technician role.

🩺 What you'll be doing:
You'll play a vital role in delivering occupational health services across sites in the Sheffield area, including:
✅ Health surveillance
✅ Wellness initiatives
✅ Audiometry, spirometry, vision testing
✅ Pre-placement health assessments
✅ Data management & reporting

🛻 This role is mobile – you'll need a full UK clean driving licence and your own vehicle. (Fuel and hotel expenses are covered!)

💼 What's in it for you?
🔹 £25,000 - £30,000 per annum (Pro Rata, DOE)
🔹 Excellent in-house benefits
🔹 Work-life balance with a 3-day week

📍 Location: South Sheffield
🕒 Type: Permanent, part-time (3 days/week)

📩 Apply directly here: https://achieva.jobswith.us/ #/jobs/35881

10/04/2025

🚨 We're Hiring: Senior DRA Clinical Trial Manager
📍 Location: Allschwil, Switzerland | 🕒 Full-Time | ⏳ 12-month contract | 🚀 Start ASAP | 💰 CHF 77.96 per hour.

Are you a detail-oriented regulatory expert with a passion for clinical research? Join our Client and take the lead on global CTA submissions, regulatory strategy, and cross-functional collaboration for clinical trials that make a real difference.

✨ What You'll Do:
🔹 Drive CTA submissions & HA interactions across Europe & internationally
🔹 Guide clinical teams with expert regulatory insight
🔹 Manage TMFs, timelines & documentation like a pro
🔹 Mentor peers, contribute to SOPs, and support import/export licensing

🧠 What You Bring:
✔ 2+ years' experience in DRA/CTA management
✔ Strong organization, communication & MS Office skills
✔ Fluent in English (other EU languages a plus!)
✔ A collaborative, detail-driven mindset

📢 Make your mark in global healthcare—apply now https://achieva.jobswith.us/ #/jobs/35879

08/04/2025

🚨 We're hiring! 🚨
Are you a hands-on scientist with a passion for early drug discovery? Want to be part of a dynamic, lab-based team pushing the boundaries of science? This could be the role for you. 👇

We're looking for a motivated Scientist (lab-based) to join our client's Cellular Assays team in Basel for a 6-month temporary cover role. You'll work alongside passionate scientists and automation experts, helping to discover the next generation of small molecule therapeutics.

🔬 𝐖𝐡𝐚𝐭 𝐲𝐨𝐮'𝐥𝐥 𝐝𝐨
✔️ Develop and optimize cellular assays
✔️ Run high-throughput screens and profile compounds
✔️ Collaborate with top-tier project teams
✔️ Translate science into action

🌟 𝐖𝐡𝐨 𝐲𝐨𝐮 𝐚𝐫𝐞
✅ Bachelor's/Master's/apprenticeship in life sciences
✅ 1–3 years' industry experience in a lab setting
✅ Skilled in cell culture, assay design, troubleshooting, and data analysis
✅ Curious, collaborative, and confident presenting your findings
✅ Fluent in English

🙌 𝐅𝐮𝐫𝐭𝐡𝐞𝐫 𝐃𝐞𝐭𝐚𝐢𝐥𝐬:
📍 Location: Basel (Onsite, 100%)
🗓️ Start Date: 1st June 2025
💼 Contract: 6 months (temporary cover)
💸 Rate: 57.97 CHF/hour
⏳ Deadline to apply: April 14, 2025 at 10:00 AM (CET)
💬 Interviews: 1–2 rounds

🔗 Interested? Apply here:

Tag someone who should see this or DM if you have questions!

07/04/2025

🚨 We're Hiring: Authentifield Library Producer | Basel, Switzerland
💼 100% workload | 💰 CHF 44.20 – 50.80/h | 📅 Start: ASAP | 📍 On-site

Join a high-impact team at the forefront of pharmaceutical forensics. You'll lead the production of spectral libraries, manage forensic samples, and help detect falsified medicines—protecting patient safety and supporting global security efforts.

We're looking for someone with 5+ years in spectroscopy or pharmaceutical analysis, strong attention to detail, and hands-on lab and data management experience.

🔬 Bachelor's or Master's in Chemistry/Spectroscopy (or equivalent experience)
🧪 Skilled with LabScanners, SAP, Chromeleon, and spectral tools
🤝 Collaborative, independent, and quality-driven

📩 Interested or know someone great? Apply Now: https://achieva.jobswith.us/ #/jobs/35876

07/04/2025

🚨 We're Hiring: Clinical Operations Manager 🚨
📍 Location: Allschwil, Switzerland
🕒 Workload: 100% Full-time
📅 Start Date: ASAP | 📆 Duration: 12 months (with potential extension)

Are you an experienced Clinical Operations professional looking to lead and shape pivotal global trials? We're seeking a Clinical Operations Manager to join our client's team and take ownership of critical trial operations across all stages—from planning and start-up to close-out.

🌟 𝐖𝐡𝐚𝐭 𝐘𝐨𝐮'𝐥𝐥 𝐁𝐞 𝐃𝐨𝐢𝐧𝐠:
- Drive the setup and management of operational trial documents, systems, and processes
- Collaborate cross-functionally on site initiations, regulatory submissions, eTMF management, and site contracts
- Lead the selection, oversight, and performance of External Service Providers (ESPs) and CROs
- Ensure timely delivery of key milestones including eCRF completion, SDV progress, and query resolution
- Act as the go-to contact for CRAs and support seamless site-level ex*****on
- Mentor junior team members and contribute to inspection readiness and trial audits
- Play a strategic role in cross-functional team meetings, investigator meetings, and site visits

✅ 𝐖𝐡𝐚𝐭 𝐖𝐞'𝐫𝐞 𝐋𝐨𝐨𝐤𝐢𝐧𝐠 𝐅𝐨𝐫:
- Degree in Life Sciences or Healthcare (BSc or equivalent)
- 4+ years of experience managing Phase II/III clinical trials
- Proven expertise in working with ESPs, budgets, and trial oversight
- Strong command of ICH-GCP and global regulatory environments
- Fluent in English with excellent communication and organizational skills
- Experience with eTMF, CTMS, and EDC systems
- Ability to travel internationally as needed

📩 Interested? Apply now https://achieva.jobswith.us/ #/jobs/35874

01/04/2025

🚨 We're Hiring: Clinical Trial Physician! 🚨

📍 Location: Allschwil, Switzerland
🕒 Schedule: Full-time | Hybrid (3 office days, 2 remote)
📅 Start Date: ASAP | Duration: 12 months

Are you an MD with 4+ years of experience in clinical research? Join our Client's team as a Clinical Trial Physician, working closely with Clinical Trial Scientists and Project Physicians to drive the success of clinical studies!

🔹 Develop expertise in the assigned therapeutic area
🔹 Contribute to clinical trial protocols, amendments, & key study documents
🔹 Provide medical oversight during trials, including safety & data review
🔹 Engage with external experts, regulatory bodies, and monitoring committees
🔹 Deliver medical training to internal teams

🎯 Requirements: MD degree, strong GCP knowledge, experience in drug development & clinical trials, and fluency in English. Cardiovascular experience is a plus!

💰 Hourly Rate: CHF 65.25 – CHF 77.96/hr
🏡 Work-life balance: Hybrid model (3 office days, 2 remote)
🌍 Global exposure: Occasional travel (approx., 1-3x per year)

Join a collaborative team and contribute to meaningful clinical research! Apply now!

🔗https://achieva.jobswith.us/ #/jobs/35869
📩

Achieva

29/04/2025

28/04/2025

24/04/2025

22/04/2025

16/04/2025

14/04/2025

14/04/2025

10/04/2025

08/04/2025

07/04/2025

07/04/2025

01/04/2025

Address

Opening Hours

Telephone

Website

Alerts

Shortcuts

Share

Category

Monday	9am - 5:30pm
Tuesday	9am - 5:30pm
Wednesday	9am - 5:30pm
Thursday	9am - 5:30pm
Friday	9am - 5pm